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(11) | EP 3 173 418 B1 |
| (12) | EUROPEAN PATENT SPECIFICATION |
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ORGANIC METAL COMPOUND, ORGANIC LIGHT-EMITTING DEVICES EMPLOYING THE SAME ORGANISCHE METALLVERBINDUNG, ORGANISCHE LICHTEMITTIERENDE VORRICHTUNGEN DAMIT COMPOSÉ MÉTALLIQUE ORGANIQUE, DISPOSITIF ÉLECTROLUMINESCENT ORGANIQUE LE COMPRENANT |
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| Note: Within nine months from the publication of the mention of the grant of the European patent, any person may give notice to the European Patent Office of opposition to the European patent granted. Notice of opposition shall be filed in a written reasoned statement. It shall not be deemed to have been filed until the opposition fee has been paid. (Art. 99(1) European Patent Convention). |
TECHNICAL FIELD
[0001] The disclosure relates to an organic metal compound and an organic light-emitting device employing the same.
BACKGROUND
[0002] An organic light-emitting diode (OLED) is a light-emitting diode employing an organic electroluminescent layer as an active layer. OLED display devices have high luminescent efficiency and long operating lifespans. In comparison with liquid-crystal displays, due to the characteristic of spontaneous emission, a device employing an organic light-emitting diode is free of a back-light source.
[0003] Generally, an organic light-emitting device is composed of a light-emission layer sandwiched between a pair of electrodes. When an electric field is applied to the electrodes, the cathode injects electrons into the light-emission layer and the anode injects holes into the light-emission layer. When the electrons recombine with the holes in the light-emission layer, excitons are formed. Recombination of the electron and hole results in light emission.
[0004] Depending on the spin states of the hole and electron, the exciton, which results from the recombination of the hole and electron, can have either a triplet or singlet spin state. Luminescence from a singlet exciton results in fluorescence whereas luminescence from a triplet exciton results in phosphorescence. The emissive efficiency of phosphorescence is three times that of fluorescence. Therefore, it is crucial to develop highly efficient phosphorescent material, in order to increase the emissive efficiency of an OLED.
SUMMARY
[0006] According to an embodiment of the disclosure, the disclosure provides an organic metal compound having a structure of Formula (I) or Formula (II):
wherein, R1 is independently hydrogen, C1-12 alkyl group, C1-12 alkoxy group, amine, C2-6 alkenyl group, C2-6 alkynyl group, C5-10 cycloalkyl group, C3-12 heteroaryl group, or C6-12 aryl group; R2, R3, R4, and R5 are independent and can be hydrogen, halogen, C1-12 alkyl group, C1-12 alkoxy group, C1-12 fluoroalkyl group, or two adjacent groups of R2, R3, R4, and R5 are optionally combined with the carbon atoms which they are attached to, to form a cycloalkyl group, or aryl group; R6 and R7 are independent and can be C1-6 alkyl group, or phenyl group; R8, R9, R10, and R11 are independent and can be hydrogen, halogen, C1-12 alkyl group, C1-12 fluoroalkyl group, or two adjacent groups of R8, R9, R10, and R11 are optionally combined with the carbon atoms which they are attached to, to form a cycloalkyl group, or aryl group; R12, R13, R14, and R15 are independent and can be hydrogen, halogen, C1-12 alkyl group, C1-12 fluoroalkyl group, or two adjacent groups of R12, R13, R14, and R15 are optionally combined with the carbon atoms which they are attached to, to form a cycloalkyl group, or aryl group; m is 1 or 2; and, n is 0 or 1.
[0007] According to another embodiment of the disclosure, the disclosure provides an organic light-emitting device, the device includes a pair of electrodes; and an organic light-emitting element disposed between the electrodes, wherein the organic light-emitting element includes the aforementioned organic metal compound.
[0008] A detailed description is given in the following embodiments with reference to the accompanying drawings.
BRIEF DESCRIPTION OF THE DRAWINGS
[0009] The disclosure can be more fully understood by reading the subsequent detailed description and examples with references made to the accompanying drawings, wherein:
FIG. 1 shows a cross section of an organic light-emitting device disclosed by an embodiment of the disclosure.
DETAILED DESCRIPTION
[0010] In the following detailed description, for purposes of explanation, numerous specific details are set forth in order to provide a thorough understanding of the disclosed embodiments. It will be apparent, however, that one or more embodiments may be practiced without these specific details. In other instances, well-known structures and devices are schematically shown in order to simplify the drawing.
[0011] According to embodiments of the disclosure, the disclosure provides an organic metal compound having a structure of Formula (I) or Formula (II):
wherein, R1 is independently hydrogen, C1-12 alkyl group, C1-12 alkoxy group, amine, C2-6 alkenyl group, C2-6 alkynyl group, C5-10 cycloalkyl group, C3-12 heteroaryl group, or C6-12 aryl group; R2, R3, R4, and R5 are independent and can be hydrogen, halogen, C1-12 alkyl group, C1-12 alkoxy group, C1-12 fluoroalkyl group, or two adjacent groups of R2, R3, R4, and R5 are optionally combined with the carbon atoms which they are attached to, to form a cycloalkyl group, or aryl group; R6 and R7 are independent and can be C1-6 alkyl group, or phenyl group; R8, R9, R10, and R11 are independent and can be hydrogen, halogen, C1-12 alkyl group, C1-12 fluoroalkyl group, or two adjacent groups of R8, R9, R10, and R11 are optionally combined with the carbon atoms which they are attached to, to form a cycloalkyl group, or aryl group; R12, R13, R14, and R15 are independent and can be hydrogen, halogen, C1-12 alkyl group, C1-12 fluoroalkyl group, or two adjacent groups of R12, R13, R14, and R15 are optionally combined with the carbon atoms which they are attached to, to form a cycloalkyl group, or aryl group; m is 1 or 2; and, n is 0 or 1. For example, R1 can be hydrogen, methyl group, ethyl group, propyl group, isopropyl group, n-butyl group, isobutyl group, tert-butyl group, pentyl group, hexyl group, cyclohexyl group, phenyl group, biphenyl group, or naphthyl group; R2, R3, R4, and R5 are independent and can be hydrogen, fluorine, methyl group, ethyl group, propyl group, isopropyl group, n-butyl group, isobutyl group, tert-butyl group, pentyl group, hexyl group, fluoromethyl, fluoroethyl, methoxy, ethoxy, propoxy, or isopropoxy or R3 and R4 are combined with the carbon atoms which they are attached to, to form a phenyl group; and, R6 and R7 are independently methyl group, ethyl group, propyl group, isopropyl group, n-butyl group, isobutyl group, tert-butyl group, pentyl group, hexyl group, or phenyl group.
[0012] According to embodiments of the disclosure, at least one of R1, R2, R3, R4, and R5 cannot be hydrogen, in order to adjust the luminescent color, increase the solubility of the compound, improve the sublimation yield, and increase the luminous efficiency and lifetime of the organic light-emitting device. According to some embodiments of the disclosure, R1 is independently hydrogen, or C1-12 alkyl group; R2, R3, R4, and R5 are independently hydrogen, halogen, C1-12 alkyl group, C1-12 alkoxy group, or two adjacent groups of R2, R3, R4, and R5 are optionally combined with the carbon atoms which they are attached to, to form an aryl group; R6 and R7 are independent C1-6 alkyl group; and, n is 0 or 1. According to embodiments of the disclosure, R8, R9, R10, and R11 are independent and can be hydrogen, fluorine, methyl group, ethyl group, propyl group, isopropyl group, n-butyl group, isobutyl group, tert-butyl group, pentyl group, hexyl group, fluoromethyl, or fluoroethyl, or R9 and R10 are combined with the carbon atoms which they are attached to, to form a phenyl group, and /or R10 and R11 are combined with the carbon atoms which they are attached to, to form a phenyl group. R12, R13, R14, and R15 are independent and can be hydrogen, fluorine, methyl group, ethyl group, propyl group, isopropyl group, n-butyl group, isobutyl group, tert-butyl group, pentyl group, hexyl group, fluoromethyl, or fluoroethyl, or R12 and R13 are combined with the carbon atoms which they are attached to, to form a phenyl group, and /or R13 and R14 are combined with the carbon atoms which they are attached to, to form a phenyl group. Herein, the term "fluoroalkyl group" means hydrogen atoms bonded on carbon atoms of alkyl group can be partially or totally replaced with fluorine. For Example, fluoromethyl can be -CH2F, -CHF2- or -CF3. According to some embodiments of the disclosure, R1 is independently hydrogen, or C1-12 alkyl group; R2, R3, R4, and R5 are independently hydrogen, halogen, C1-12 alkyl group, C1-12 alkoxy group, or two adjacent groups of R2, R3, R4, and R5 are optionally combined with the carbon atoms which they are attached to, to form an aryl group; R8, R9, R10, and R11 are independently hydrogen, C1-12 alkyl group, or two adjacent groups of R8, R9, R10, and R11 are optionally combined with the carbon atoms which they are attached to, to form an aryl group; R12, R13, R14, and R15 are independently hydrogen, or C1-12 alkyl group; and, m is 1 or 2.
[0013] The organic metal compounds of the disclosure can serve as a green phosphorescent dopant material, and can be applied to an organic light-emitting device for enhancing the luminous efficiency and lifetime.
[0014] According to some embodiments of the disclosure, the organic metal compound can be
R2, R3, R4, and R5 are independent and can be hydrogen, halogen, C1-12 alkyl group, C1-12 alkoxy group, C1-12 fluoroalkyl group, or two adjacent groups of R2, R3, R4, and R5 are optionally combined with the carbon atoms which they are attached to, to form a cycloalkyl group, or aryl group; R6 and R7 are independent C1-6 alkyl group, or phenyl group; and, n is 0, or 1. For example, R2, R3, R4, and R5 are independently hydrogen, fluorine, methyl group, ethyl group, propyl group, isopropyl group, n-butyl group, isobutyl group, tert-butyl group, pentyl group, hexyl group, fluoromethyl, fluoroethyl, methoxy, ethoxy, propoxy, or isopropoxy. Furthermore, R3 and R4 can be combined with the carbon atoms which they are attached to, to form a phenyl group. R6 and R7 can be independently methyl group, ethyl group, propyl group, isopropyl group, n-butyl group, isobutyl group, tert-butyl group, pentyl group, hexyl group, or phenyl group. According to embodiments of the disclosure, R2, R3, R4, and R5 cannot be hydrogen.
[0015] According to some embodiments of the disclosure, the organic metal compound can be
or,
R1 is independent and can be hydrogen, C1-12 alkyl group, C1-12 alkoxy group, amine, C2-6 alkenyl group, C2-6 alkynyl group, C5-10 cycloalkyl group, C3-12 heteroaryl group, or C6-12 aryl group; and, R2, R3, R4, and R5 are independent and can be hydrogen, halogen, C1-12 alkyl group, C1-12 alkoxy group, C1-12 fluoroalkyl group, or two adjacent groups of R2, R3, R4, and R5 are optionally combined with the carbon atoms which they are attached to, to form a cycloalkyl group, or aryl group. For example, R1 can be hydrogen, methyl group, ethyl group, propyl group, isopropyl group, n-butyl group, isobutyl group, tert-butyl group, pentyl group, hexyl group, cyclohexyl group, phenyl group, biphenyl group, or naphthyl group. For example, R2, R3, R4, and R5 are independently hydrogen, fluorine, methyl group, ethyl group, propyl group, isopropyl group, n-butyl group, isobutyl group, tert-butyl group, pentyl group, hexyl group, fluoromethyl, fluoroethyl, methoxy, ethoxy, propoxy, or isopropoxy. Furthermore, R3 and R4 can be combined with the carbon atoms which they are attached to, to form a phenyl group. According to embodiments of the disclosure, R1, R2, R3, R4, and R5 cannot be hydrogen.
[0016] According to some embodiments of the disclosure, the organic metal compound can be
R1 is independent and can be hydrogen, C1-12 alkyl group, C1-12 alkoxy group, amine, C2-6 alkenyl group, C2-6 alkynyl group, C5-10 cycloalkyl group, C3-12 heteroaryl group, or C6-12 aryl group; and, R2, R3, R4, and R5 are independent and can be hydrogen, halogen, C1-12 alkyl group, C1-12 alkoxy group, C1-12 fluoroalkyl group, or two adjacent groups of R2, R3, R4, and R5 are optionally combined with the carbon atoms which they are attached to, to form a cycloalkyl group, or aryl group. For example, R1 can be hydrogen, methyl group, ethyl group, propyl group, isopropyl group, n-butyl group, isobutyl group, tert-butyl group, pentyl group, hexyl group, cyclohexyl group, phenyl group, biphenyl group, or naphthyl group. For example, R2, R3, R4, and R5 are independently hydrogen, fluorine, methyl group, ethyl group, propyl group, isopropyl group, n-butyl group, isobutyl group, tert-butyl group, pentyl group, hexyl group, fluoromethyl, fluoroethyl, methoxy, ethoxy, propoxy, or isopropoxy. Furthermore, R3 and R4 can be combined with the carbon atoms which they are attached to, to form a phenyl group. According to embodiments of the disclosure, R1, R2, R3, R4, and R5 cannot be hydrogen.
[0018] According to some embodiments of the disclosure, the organic metal compound can be
R1 is independent and can be hydrogen, C1-12 alkyl group, C1-12 alkoxy group, amine, C2-6 alkenyl group, C2-6 alkynyl group, C5-10 cycloalkyl group, C3-12 heteroaryl group, or C6-12 aryl group; and, R2, R3, R4, and R5 are independent and can be hydrogen, halogen, C1-12 alkyl group, C1-12 alkoxy group, C1-12 fluoroalkyl group, or two adjacent groups of R2, R3, R4, and R5 are optionally combined with the carbon atoms which they are attached to, to form a cycloalkyl group, or aryl group. For example, R1 can be hydrogen, methyl group, ethyl group, propyl group, isopropyl group, n-butyl group, isobutyl group, tert-butyl group, pentyl group, hexyl group, cyclohexyl group, phenyl group, biphenyl group, or naphthyl group. For example, R2, R3, R4, and R5 are independently hydrogen, fluorine, methyl group, ethyl group, propyl group, isopropyl group, n-butyl group, isobutyl group, tert-butyl group, pentyl group, hexyl group, fluoromethyl, fluoroethyl, methoxy, ethoxy, propoxy, or isopropoxy. Furthermore, R3 and R4 can be combined with the carbon atoms which they are attached to, to form a phenyl group. According to embodiments of the disclosure, R1, R2, R3, R4, and R5 cannot be hydrogen, and m can be 1 or 2.
[0019] According to some embodiments of the disclosure, the organic metal compound can be
R1 is independent and can be hydrogen, C1-12 alkyl group, C1-12 alkoxy group, amine, C2-6 alkenyl group, C2-6 alkynyl group, C5-10 cycloalkyl group, C3-12 heteroaryl group, or C6-12 aryl group; and, R2, R3, R4, and R5 are independent and can be hydrogen, halogen, C1-12 alkyl group, C1-12 alkoxy group, C1-12 fluoroalkyl group, or two adjacent groups of R2, R3, R4, and R5 are optionally combined with the carbon atoms which they are attached to, to form a cycloalkyl group, or aryl group. For example, R1 can be hydrogen, methyl group, ethyl group, propyl group, isopropyl group, n-butyl group, isobutyl group, tert-butyl group, pentyl group, hexyl group, cyclohexyl group, phenyl group, biphenyl group, or naphthyl group. For example, R2, R3, R4, and R5 are independently hydrogen, fluorine, methyl group, ethyl group, propyl group, isopropyl group, n-butyl group, isobutyl group, tert-butyl group, pentyl group, hexyl group, fluoromethyl, fluoroethyl, methoxy, ethoxy, propoxy, or isopropoxy. Furthermore, R3 and R4 can be combined with the carbon atoms which they are attached to, to form a phenyl group. According to embodiments of the disclosure, R1, R2, R3, R4, and R5 cannot be hydrogen. R8, R9, R10, and R11 are independent and can be hydrogen, halogen, C1-12 alkyl group, C1-12 fluoroalkyl group, or two adjacent groups of R8, R9, R10, and R11 are optionally combined with the carbon atoms which they are attached to, to form a cycloalkyl group, or aryl group. For example, R8, R9, R10, and R11 are independent and can be hydrogen, fluorine, methyl group, ethyl group, propyl group, isopropyl group, n-butyl group, isobutyl group, tert-butyl group, pentyl group, hexyl group, fluoromethyl, or fluoroethyl, or R9 and R10 are combined with the carbon atoms which they are attached to, to form a phenyl group, and /or R10 and R11 are combined with the carbon atoms which they are attached to, to form a phenyl group, and m can be 1 or 2.
[0020] According to some embodiments of the disclosure, the organic metal compound can be
be hydrogen, C1-12 alkyl group, C1-12 alkoxy group, amine, C2-6 alkenyl group, C2-6 alkynyl group, C5-10 cycloalkyl group, C3-12 heteroaryl group, or C6-12 aryl group; and, R2, R3, R4, and R5 are independent and can be hydrogen, halogen, C1-12 alkyl group, C1-12 alkoxy group, C1-12 fluoroalkyl group, or two adjacent groups of R2, R3, R4, and R5 are optionally combined with the carbon atoms which they are attached to, to form a cycloalkyl group, or aryl group. For example, R1 can be hydrogen, methyl group, ethyl group, propyl group, isopropyl group, n-butyl group, isobutyl group, tert-butyl group, pentyl group, hexyl group, cyclohexyl group, phenyl group, biphenyl group, or naphthyl group. For example, R2, R3, R4, and R5 are independently hydrogen, fluorine, methyl group, ethyl group, propyl group, isopropyl group, n-butyl group, isobutyl group, tert-butyl group, pentyl group, hexyl group, fluoromethyl, fluoroethyl, methoxy, ethoxy, propoxy, or isopropoxy. Furthermore, R3 and R4 can be combined with the carbon atoms which they are attached to, to form a phenyl group. According to embodiments of the disclosure, R1, R2, R3, R4, and R5 cannot be hydrogen. R12, R13, R14, and R15 are independent and can be hydrogen, halogen, C1-12 alkyl group, C1-12 fluoroalkyl group, or two adjacent groups of R12, R13, R14, and R15 are optionally combined with the carbon atoms which they are attached to, to form a cycloalkyl group, or aryl group. For example, R12, R13, R14, and R15 are independent and can be hydrogen, fluorine, methyl group, ethyl group, propyl group, isopropyl group, n-butyl group, isobutyl group, tert-butyl group, pentyl group, hexyl group, fluoromethyl, or fluoroethyl, or R12 and R13 are combined with the carbon atoms which they are attached to, to form a phenyl group, and /or R13 and R14 are combined with the carbon atoms which they are attached to, to form a phenyl group, and m can be 1 or 2.
[0021] According to some embodiments of the disclosure, the organic metal compound can be
R1 is independent and can be hydrogen, C1-12 alkyl group, C1-12 alkoxy group, amine, C2-6 alkenyl group, C2-6 alkynyl group, C5-10 cycloalkyl group, C3-12 heteroaryl group, or C6-12 aryl group; and, R2, R3, R4, and R5 are independent and can be hydrogen, halogen, C1-12 alkyl group, C1-12 alkoxy group, C1-12 fluoroalkyl group, or two adjacent groups of R2, R3, R4, and R5 are optionally combined with the carbon atoms which they are attached to, to form a cycloalkyl group, or aryl group. For example, R1 can be hydrogen, methyl group, ethyl group, propyl group, isopropyl group, n-butyl group, isobutyl group, tert-butyl group, pentyl group, hexyl group, cyclohexyl group, phenyl group, biphenyl group, or naphthyl group. For example, R2, R3, R4, and R5 are independently hydrogen, fluorine, methyl group, ethyl group, propyl group, isopropyl group, n-butyl group, isobutyl group, tert-butyl group, pentyl group, hexyl group, fluoromethyl, fluoroethyl, methoxy, ethoxy, propoxy, or isopropoxy. Furthermore, R3 and R4 can be combined with the carbon atoms which they are attached to, to form a phenyl group. According to embodiments of the disclosure, R1, R2, R3, R4, and R5 cannot be hydrogen. R12, R13, R14, and R15 are independent and can be hydrogen, halogen, C1-12 alkyl group, C1-12 fluoroalkyl group, or two adjacent groups of R12, R13, R14, and R15 are optionally combined with the carbon atoms which they are attached to, to form a cycloalkyl group, or aryl group. For example, R12, R13, R14, and R15 are independent and can be hydrogen, fluorine, methyl group, ethyl group, propyl group, isopropyl group, n-butyl group, isobutyl group, tert-butyl group, pentyl group, hexyl group, fluoromethyl, or fluoroethyl, or R12 and R13 are combined with the carbon atoms which they are attached to, to form a phenyl group, and /or R13 and R14 are combined with the carbon atoms which they are attached to, to form a phenyl group, and m can be 1 or 2.
[0023] The following examples are intended to illustrate the disclosure more fully without limiting the scope, since numerous modifications and variations will be apparent to those skilled in this art.
Example 1 : Preparation of Organic metal compound (I)
[0025] 130 mmol of nitromethane, 52 mmol of 2-furfural, and 10 ml of methanol were added into a reaction bottle. Next, 130 mL of sodium hydroxide aqueous solution (1M) were dropwisely added into the reaction bottle at 0°C. After stirring at 0°C for 15 min, the mixture was added slowly into a hydrochloric acid aqueous solution (50 ml, 8 M). Next, the reaction was terminated after being checked by thin layer chromatography (TLC), and the result was added into a reaction bottle with CH2Cl2 and brine. After extracting, the organic phase was collected. Next, an organic phase was separated and concentrated, and then dried by anhydrous magnesium sulfate. Finally, the result was purified by column chromatography with petroleum ether and ethyl acetate, obtaining Compound (I) with a yield of 93%. The synthesis pathway of the above reaction was as follows:
[0026] The physical measurement of the compound (I) is listed below: 1H-NMR (200 MHz, CDCl3, δ): 7.77 (d, 1H), 7.59 (s, 1H), 7.53 (d, 1H), 6.89 (d, 1H), 6.57 (dd, 1H).
[0027] Next, 30 ml of ethyl ether and 81 mmol of lithium aluminium hydride were added into a reaction bottle. After stirring at 0°C, 27 mmol of compound (I) and 50 ml of ethyl ether was added slowly into the reaction bottle at 0°C. After stirring for 10 min, the reaction bottle was heated to room temperature and then heated to reflux for 8 hr. Next, the reaction bottle was cooled to 0°C, and then water was added slowly to quench reaction. Next, sodium hydroxide aqueous solution (10 wt%) was added into the reaction bottle. After diluting with ethyl ether, filtrating, and concentrating, compound (II) is obtained. The synthesis pathway of the above reaction was as follows:
[0028] Next, 55.1 mmol of compound (II), and 200 ml of water were added into a reaction bottle. Next, 82.5 mmol of 4-methylbenzoyl chloride was added into the reaction bottle at 0°C. After the addition was complete, sodium hydroxide aqueous solution (20 wt%) was added into the reaction bottle. After stirring for 8 hr and filtrating, compound (III) was obtained. The synthesis pathway of the above reaction was as follows:
[0029] Next, 10 mmol of compound (III), 20 ml of toluene, and 3 mmol of phosphorus oxychloride (POCl3) were added into the reaction bottle. After heating the reaction bottle for 2 hr, the mixture was neutralized by saturated sodium bicarbonate aqueous solution, and extracted with toluene. After concentrating, Compound (IV) was obtained. The synthesis pathway of the above reaction was as follows:
[0030] Next, 10 mmol of Compound (IV), 0.5g of palladium 10% on carbon (Pd/C catalyst), and 100 ml of toluene were added into a reaction bottle. Next, the reaction bottle was heated to reflux for 18 hr. Next, after removing Pd/C catalyst by filtration, the filtrate was extracted three times using ethyl acetate (EA) and water as the extraction solvent, and an organic phase was separated and concentrated, and then purified by column chromatography, obtaining Compound (V) with a yield of 92%. The synthesis pathway of the above reaction was as follows:
[0031] The physical measurement of the Compound (V) is listed below: 1H-NMR (200 MHz, CDCl3, δ): 8.56-8.53 (d, 1H), 7.86-7.82 (d, 2H), 7.66-7.65 (m, 1H), 7.39-7.36 (d, 1H), 7.33-7.29 (d, 2H), 7.05-7.04 (m, 1H), 2.42 (s, 3H).
[0032] Next, 1.54 mmol of Compound (V), iridium trichloride (IrCl3) (0.7 mmol), 15 ml of 2-methoxyethanol, and 5 ml of water were added into the reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to reflux. After reacting for 24 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected, washed with water and methanol, and dried, obtaining Compound (VI). The synthesis pathway of the above reaction was as follows:
[0033] Next, 1 mmol of Compound (VI), 3 mmol of acetylacetone, 2 mmol of sodium carbonate, and 10 ml of 2-methoxyethanol were added into a reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to 120 °C. After reacting for 12 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected and washed with water and hexane, and then dissolved in dichloromethane. Next, the solution was extracted three times using dichloromethane and water. Next, an organic phase was separated and concentrated, and then purified by column chromatography, obtaining Organic metal compound (I) with a yield of 50%. The synthesis pathway of the above reaction was as follows:
[0034] The physical measurement of Organic metal compound (I) is listed below: 1H-NMR (200 MHz, CDCl3, δ): 8.40-8.37 (d, 2H), 7.83-7.79 (m, 4H), 7.51-7.50 (s, 2H), 7.32-7.28 (d, 2H), 6.70-6.66 (d, 2H), 6.09 (s, 2H), 5.19 (s, 1H), 2.03 (s, 6H), 1.75 (s, 6H).
Example 2 : Preparation of Organic metal compound (II)
[0036] First, 55.1 mmol of Compound (II), and 200 ml of water were added into a reaction bottle. Next, 82.5 mmol of 2,4-difluorobenzoyl chloride was added into the reaction bottle at 0°C. After the addition was complete, sodium hydroxide aqueous solution (20 wt%) was added into the reaction bottle. After stirring for 8 hr, the mixture was filtrated, obtaining Compound (VII). The synthesis pathway of the above reaction was as follows:
[0037] Next, 10 mmol of Compound (VII), 20 ml of toluene, and 3 mmol of phosphorus oxychloride (POCl3) were added into the reaction bottle. After heating the reaction bottle for 2 hr, the mixture was neutralized by saturated sodium bicarbonate aqueous solution, and extracted with toluene. After concentrating, Compound (VIII) was obtained. The synthesis pathway of the above reaction was as follows:
[0038] Next, 10 mmol of Compound (VIII), 0.5g of palladium 10% on carbon (Pd/C catalyst), and 100 ml of toluene were added into the reaction bottle. Next, the reaction bottle was heated to reflux for 18 hr. Next, after removing Pd/C catalyst by filtration, the filtrate was extracted three times using ethyl acetate (EA) and water as the extraction solvent, and an organic phase was separated and concentrated, and then purified by column chromatography, obtaining Compound (IX) with a yield of 95%. The synthesis pathway of the above reaction was as follows:
[0039] The physical measurement of Compound (IX) is listed below: 1H-NMR (200 MHz, CDCl3, δ): 8.61-8.58 (d, 1H), 7.84-7.72 (m, 1H), 7.70-7.68 (d, 1H), 7.49-7.46 (d, 1H), 7.09-6.92 (m, 2H), 6.83-6.80 (m, 1H)
[0040] Next, Compound (IX) (1.54 mmol), and 0.7 mmol of iridium trichloride (IrCl3), 15 ml of 2-methoxyethanol, and 5 ml of water were added into the reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to reflux. After reacting for 24 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected, washed with water and methanol, and dried, obtaining (X). The synthesis pathway of the above reaction was as follows:
[0041] Next, 1 mmol of Compound (X), 3 mmol of acetylacetone, 2 mmol of sodium carbonate (Na2CO3), and 10 ml of 2-methoxyethanol were added into a reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to 120 °C. After reacting for 12 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected and washed with water and hexane, and then dissolved in dichloromethane. Next, the solution was extracted three times using dichloromethane and water. Next, an organic phase was separated and concentrated, and then purified by column chromatography, obtaining Organic metal compound (II) with a yield of 45%. The synthesis pathway of the above reaction was as follows:
[0042] The physical measurement of Organic metal compound (II) is listed below: 1H-NMR (200 MHz, CDCl3, δ): 8.40-8.37 (d, 2H), 7.76-7.75 (m, 2H), 7.55 (m, 2H), 7.43-7.40 (d, 2H), 6.41-6.31 (m, 2H), 5.67-5.61 (m, 2H), 5.24 (s, 1H), 1.78 (s, 6H).
Example 3: Preparation of Organic metal compound (III)
[0044] 55.1 mmol of Compound (II), and 200 ml of water were added into the reaction bottle. Next, 82.5 mmol of 4-tert-Butylbenzoyl chloride was added into the reaction bottle at 0°C. After the addition was complete, sodium hydroxide aqueous solution (20 wt%) was added into the reaction bottle. After stirring for 8 hr, the mixture was filtrated, obtaining Compound (XI). The synthesis pathway of the above reaction was as follows:
[0045] Next, 10 mmol of Compound (XI), 20 ml of toluene, and 3 mmol of phosphorus oxychloride (POCl3) were added into the reaction bottle. After heating the reaction bottle for 2 hr, the mixture was neutralized by saturated sodium bicarbonate aqueous solution, and extracted with toluene. After concentrating, Compound (XII) was obtained. The synthesis pathway of the above reaction was as follows:
[0046] Next, 10 mmol of Compound (XII), 0.5g of palladium 10% on carbon (Pd/C catalyst), and 100 ml of toluene were added into the reaction bottle. Next, the reaction bottle was heated to reflux for 18 hr. Next, after removing Pd/C catalyst by filtration, the filtrate was extracted three times using ethyl acetate (EA) and water as the extraction solvent, and an organic phase was separated and concentrated, and then purified by column chromatography, obtaining Compound (XIII) with a yield of 75%. The synthesis pathway of the above reaction was as follows:
[0047] The physical measurement of Compound (XIII) is listed below: 1H-NMR (200 MHz, CDCl3, δ): 8.58-8.55 (d, 1H), 7.92-7.88 (d, 2H), 7.70-7.69 (m, 1H), 7.68 (m, 1H), 7.57-7.53 (d, 2H), 7.42-7.38 (d, 1H), 7.10-7.09 (s, 1H), 1.38 (s, 9H).
[0048] Next, 1.54 mmol of Compound (XIII), and 0.7 mmol of iridium trichloride (IrCl3), 15 ml of 2-methoxyethanol, and 5 ml of water were added into the reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to reflux. After reacting for 24 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected, washed with water and methanol, and dried, obtaining Compound (XIV). The synthesis pathway of the above reaction was as follows:
[0049] Next, 1 mmol of Compound (XIV), 3 mmol of acetylacetone, 2 mmol of sodium carbonate (Na2CO3), and 10 ml of 2-methoxyethanol were added into a reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to 120 °C. After reacting for 12 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected and washed with water and hexane, and then dissolved in dichloromethane. Next, the solution was extracted three times using dichloromethane and water. Next, an organic phase was separated and concentrated, and then purified by column chromatography, obtaining Organic metal compound (III) with a yield of 54%. The synthesis pathway of the above reaction was as follows:
[0050] The physical measurement of Organic metal compound (III) is listed below 1H-NMR (200 MHz, CDCl3, δ): 8.44-8.41 (d, 2H), 7.83-7.78 (m, 4H), 7.50-7.49 (m, 2H), 7.35-7.32 (d, 2H), 6.92-6.87 (m, 2H), 6.22-6.21 (m, 2H), 5.29 (s, 1H), 1.77 (s, 6H), 0.99 (s, 9H).
Example 4: Preparation of Organic metal compound (IV)
[0052] 55.1 mmol of Compound (II), and 200 ml of water were added into the reaction bottle. Next, 82.5 mmol of benzoyl chloride was added into the reaction bottle at 0°C. After the addition was complete, sodium hydroxide aqueous solution (20 wt%) was added into the reaction bottle. After stirring for 8 hr, the mixture was filtrated, obtaining Compound (XV). The synthesis pathway of the above reaction was as follows:
[0053] Next, 10 mmol Compound (XV), 20 ml of toluene, and 3 mmol of phosphorus oxychloride (POCl3) were added into the reaction bottle. After heating the reaction bottle for 2 hr, the mixture was neutralized by saturated sodium bicarbonate aqueous solution, and extracted with toluene. After concentrating, Compound (XVI) was obtained. The synthesis pathway of the above reaction was as follows:
[0054] Next, Compound (XVI) (10 mmol), 0.5g of palladium 10% on carbon (Pd/C catalyst), and 100 ml of toluene were added into the reaction bottle. Next, the reaction bottle was heated to reflux for 18 hr. Next, after removing Pd/C catalyst by filtration, the filtrate was extracted three times using ethyl acetate (EA) and water as the extraction solvent, and an organic phase was separated and concentrated, and then purified by column chromatography, obtaining Compound (XVII) with a yield of 96%. The synthesis pathway of the above reaction was as follows:
[0055] The physical measurement of Compound (XVII) is listed below: 1H-NMR (200 MHz, CDCl3, δ): 8.61 (d, 1H), 7.98-7.94 (d, 2H), 7.71-7.70 (s, 1H), 7.58-7.42 (m, 5H), 7.09 (s, 1H).
[0056] Next, 1.54 mmol of Compound (XVII), and 0.7 mmol of iridium trichloride (IrCl3), 15 ml of 2-methoxyethanol, and 5 ml of water were added into the reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to reflux. After reacting for 24 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected, washed with water and methanol, and dried, obtaining Compound (XVIII). The synthesis pathway of the above reaction was as follows:
[0057] Next, 1 mmol of Compound (XVIII), 3 mmol of acetylacetone, 2 mmol of sodium carbonate (Na2CO3), and 10 ml of 2-methoxyethanol were added into a reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to 120 °C. After reacting for 12 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected and washed with water and hexane, and then dissolved in dichloromethane. Next, the solution was extracted three times using dichloromethane and water. Next, an organic phase was separated and concentrated, and then purified by column chromatography, obtaining Organic metal compound (IV) with a yield of 46%. The synthesis pathway of the above reaction was as follows:
[0058] The physical measurement of Organic metal compound (IV) is listed below 1H-NMR (200 MHz, CDCl3, δ): 8.45-8.42 (d, 2H), 7.94-7.90 (d, 2H), 7.80 (m, 2H), 7.52 (m, 2H), 7.37-7.33 (d, 2H), 6.89-6.82 (t, 2H), 6.68-6.61 (t, 2H), 6.29-6.25 (d, 2H), 5.22 (s, 1H), 1.77 (s, 3H).
Example 5: Preparation of Organic metal compound (V)
[0060] 1 mmol of Organic metal compound (IV), 2 mmol of Compound (XVII), and 15 mL of glycerol were added into a reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to 200 °C. After reacting for 48 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected and washed with water and dichloromethane, and then purified by column chromatography, obtaining Organic metal compound (V) with a yield of 47%. The synthesis pathway of the above reaction was as follows:
[0061] The physical measurement of Organic metal compound (V) is listed below 1H-NMR (200 MHz, CDCl3, δ): 8.05-8.02 (d, 3H), 7.73-7.72 (m, 3H), 7.54-7.40 (m, 3H), 7.40-7.37 (d, 3H), 7.05-6.82 (m, 12H).
Example 6: Preparation of Organic metal compound (VI)
[0063] 55.1 mmol of Compound (II), and 200 ml of water were added into the reaction bottle. Next, 82.5 mmol of 2-naphthoyl chloride were added into the reaction bottle at 0°C. After the addition was complete, sodium hydroxide aqueous solution (20wt%) was added into the reaction bottle. After stirring for 8 hr, the mixture was filtrated, obtaining Compound (XIX). The synthesis pathway of the above reaction was as follows:
[0064] Next, 10 mmol of Compound (XIX), 20 ml of toluene, and 3 mmol of phosphorus oxychloride (POCl3) were added into the reaction bottle. After heating the reaction bottle for 2 hr, the mixture was neutralized by saturated sodium bicarbonate aqueous solution, and extracted with toluene. After concentrating, Compound (XX) is obtained. The synthesis pathway of the above reaction was as follows:
[0065] Next, 10 mmol of Compound (XX), 0.5g of palladium 10% on carbon (Pd/C catalyst), and 100 ml of toluene were added into the reaction bottle. Next, the reaction bottle was heated to reflux for 18 hr. Next, after removing Pd/C catalyst by filtration, the filtrate was extracted three times using ethyl acetate (EA) and water as the extraction solvent, and an organic phase was separated and concentrated, and then purified by column chromatography, obtaining Compound (XXI) with a yield of 72%. The synthesis pathway of the above reaction was as follows:
[0066] The physical measurement of Compound (XXI) is listed below: 1H-NMR (200 MHz, CDCl3, δ): 8.66-8.63 (d, 1H), 8.42 (s, 1H), 8.14-7.89 (m, 4H), 7.74-7.72 (d, 1H), 7.56-7.44 (m, 3H), 7.17 (s, 1H).
[0067] Next, Compound (XXI) (1.54 mmol), and 0.7 mmol of iridium trichloride (IrCl3), 15 ml of 2-methoxyethanol, and 5 ml of water were added into the reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to reflux. After reacting for 24 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected, washed with water and methanol, and dried, obtaining Compound (XXII). The synthesis pathway of the above reaction was as follows:
[0068] Next, 1 mmol of Compound (XXII), 3 mmol of acetylacetone, 2 mmol of sodium carbonate (Na2CO3), and 10 ml of 2-methoxyethanol were added into a reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to 120 °C. After reacting for 12 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected and washed with water and hexane, and then dissolved in dichloromethane. Next, the solution was extracted three times using dichloromethane and water. Next, an organic phase was separated and concentrated, and then purified by column chromatography, obtaining Organic metal compound (VI) with a yield of 48%. The synthesis pathway of the above reaction was as follows:
[0069] The physical measurement of Organic metal compound (VI) is listed below 1H-NMR (200 MHz, CDCl3, δ): 8.60-8.57 (d, 2H), 8.42 (s, 2H), 7.92 (m, 2H), 7.91 (m, 2H), 7.77-7.65 (m, 2H), 7.48-7.45 (d, 2H), 7.16-6.60 (m, 6H), 6.60 (s, 2H), 5.25 (s, 1H), 1.77 (s, 6H).
Example 7: Preparation of Organic metal compound (VII)
[0071] 130 mmol of nitromethane, 52 mmol of 5-methyl-2-furaldehyde, and 10 ml methanol were added into a reaction bottle. Next, 130 mL of sodium hydroxide aqueous solution (1 M) were dropwisely added into the reaction bottle at 0°C. After stirring at 0°C for 15 min, the mixture was added slowly into a hydrochloric acid aqueous solution (50 ml, 8 M). Next, the reaction was terminated after being checked by thin layer chromatography (TLC), and the result was added into a reaction bottle with CH2Cl2 and brine. After extracting, the organic phase was collected. Next, an organic phase was separated and concentrated, and then dried by anhydrous magnesium sulfate. Finally, the result was purified by column chromatography with petroleum ether and ethyl acetate, obtaining Compound (XXIII) with a yield of 70%.
[0072] 55.1 mmol of Compound (XXIII), and 200 ml of water were added into the reaction bottle. Next, 82.5 mmol of 2,4-difluorobenzoyl chloride was added into the reaction bottle at 0°C. After the addition was complete, sodium hydroxide aqueous solution (20 wt%) was added into the reaction bottle. After stirring for 8 hr, the mixture was filtrated, obtaining Compound (XXIV). The synthesis pathway of the above reaction was as follows:
[0073] Next, 10 mmol of Compound (XXIV), 20 ml of toluene, and 3 mmol of phosphorus oxychloride (POCl3) were added into the reaction bottle. After heating the reaction bottle for 2 hr, the mixture was neutralized by saturated sodium bicarbonate aqueous solution, and extracted with toluene. After concentrating, Compound (XXV) was obtained. The synthesis pathway of the above reaction was as follows:
[0074] Next, 10 mmol of Compound (XXV), 0.5g of palladium 10% on carbon (Pd/C catalyst), and 100 ml of toluene were added into the reaction bottle. Next, the reaction bottle was heated to reflux for 18 hr. Next, after removing Pd/C catalyst by filtration, the filtrate was extracted three times using ethyl acetate (EA) and water as the extraction solvent, and an organic phase was separated and concentrated, and then purified by column chromatography, obtaining Compound (XXVI) with a yield of 71%. The synthesis pathway of the above reaction was as follows:
[0075] The physical measurement of Compound (XXVI) is listed below: 1H-NMR (200 MHz, CDCl3, δ): 8.54-8.51 (d, 1H), 7.82-7.73 (q, 1H), 7.38-7.36 (d, 1H), 7.09-6.91 (m, 2H), 6.43-6.40 (d, 1H), 2.50 (s, 3H).
[0076] Next, 1.54 mmol of Compound (XXVI), and 0.7 mmol of iridium trichloride (IrCl3), 15 ml of 2-methoxyethanol, and 5 ml of water were added into the reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to reflux. After reacting for 24 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected, washed with water and methanol, and dried, obtaining Compound (XXVII). The synthesis pathway of the above reaction was as follows:
[0077] Next, 1 mmol of Compound (XXVII), 3 mmol of acetylacetone, 2 mmol of sodium carbonate (Na2CO3), and 10 ml of 2-methoxyethanol were added into a reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to 120 °C. After reacting for 12 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected and washed with water and hexane, and then dissolved in dichloromethane. Next, the solution was extracted three times using dichloromethane and water. Next, an organic phase was separated and concentrated, and then purified by column chromatography, obtaining Organic metal compound (VII) with a yield of 50%. The synthesis pathway of the above reaction was as follows:
[0078] The physical measurement of Organic metal compound (VII) is listed below: 1H-NMR (200 MHz, CDCl3, δ): 8.33-8.30 (d, 2H), 7.32-7.28 (d, 2H), 7.14-7.12 (m, 2H), 6.39-6.26 (m, 2H), 5.64-5.59 (m, 2H), 5.23 (s, 1H), 2.58 (s, 6H), 1.77 (s, 6H).
Example 8: Preparation of Organic metal compound (VIII)
[0080] Next, 1 mmol of Compound (XIV), 3 mmol of 2,2,6,6-tetramethylheptane-3,5-dione, 2 mmol of sodium carbonate (Na2CO3), and 10 ml of 2-methoxyethanol were added into a reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to 120 °C. After reacting for 12 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected and washed with water and hexane, and then dissolved in dichloromethane. Next, the solution was extracted three times using dichloromethane and water. Next, an organic phase was separated and concentrated, and then purified by column chromatography, obtaining Organic metal compound (VIII) with a yield of 56%. The synthesis pathway of the above reaction was as follows:
[0081] The physical measurement of Organic metal compound (VIII) is listed below 1H-NMR (200 MHz, CDCl3, δ): 8.34-8.31 (d, 2H), 7.83-7.75 (m, 4H), 7.50-7.49 (m, 2H), 7.26-7.23 (d, 2H), 6.91-6.86 (d, 2H), 6.36 (m, 2H), 5.44 (s, 1H), 1.52 (s, 9H), 1.02 (s, 9H), 0.95 (s, 9H).
Example 9: Preparation of Organic metal compound (IX)
[0083] 1 mmol of Organic metal compound (III), 1 mmol of Compound (XIII), and 15 mL of glycerol were added into a reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to 200 °C. After reacting for 48 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected and washed with water and dichloromethane, and then purified by column chromatography, obtaining Organic metal compound (IX) with a yield of 35%. The synthesis pathway of the above reaction was as follows:
[0084] The physical measurement of Organic metal compound (IX) is listed below 1H-NMR (200 MHz, CDCl3, δ): 7.94-7.90 (d, 3H), 7.68 (d, 3H), 7.49 (d, 3H), 7.38-7.35 (d, 3H), 7.02-6.95 (m, 9H), 1.10 (s, 27H).
Example 10: Preparation of Organic metal compound (X)
[0086] 1 mmol of Organic metal compound (I), 2 mmol of Compound (V), and 15 mL of glycerol were added into a reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to 200 °C. After reacting for 48 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected and washed with water and ethyl acetate (EA), and then purified by column chromatography, obtaining Organic metal compound (X). The synthesis pathway of the above reaction was as follows:
[0087] The physical measurement of Organic metal compound (X) is listed below 1H NMR (200 MHz, CDCl3, 294 K): 7.92 (d, 3H), 7.70 (d, 3H), 7.52 (d, 3H), 7.32 (d, 3H), 6.97 (d, 3H), 6.77∼6.74 (m, 6H), 2.14 (s, 9H).
Example 11: Preparation of Organic metal compound (XI)
[0089] 1 mmol of Organic metal compound (II), 2 mmol of Compound (IX), and 15 mL of glycerol were added into a reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to 200 °C. After reacting for 48 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected and washed with water and ethyl acetate (EA), and then purified by column chromatography, obtaining Organic metal compound (XI). The synthesis pathway of the above reaction was as follows:
[0090] The physical measurement of Organic metal compound (XI) is listed below 1H NMR (200 MHz, CDCl3, 294 K): 7.70 (d, 3H), 7.49 (s, 3H), 7.34 (d, 3H), 7.11 (d, 3H), 6.48∼6.28 (m, 6H).
Example 12: Preparation of Organic metal compound (XII)
[0092] 4.2 mmol of Compound (XXX), 2 mmol of iridium trichloride (IrCl3), 15 ml of 2-methoxyethanol, and 5 ml of water were added into the reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to reflux. After reacting for 24 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected, washed with water and methanol, and dried, obtaining Compound (XXXI). The synthesis pathway of the above reaction was as follows:
[0093] Next, 1 mmol of Compound (XXXI), 3 mmol of acetylacetone, 2 mmol of sodium carbonate (Na2CO3), and 10 ml of 2-methoxyethanol were added into a reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to 120 °C. After reacting for 12 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected and washed with water and hexane, and then dissolved in dichloromethane. Next, the solution was extracted three times using dichloromethane and water. Next, an organic phase was separated and concentrated, and then purified by column chromatography, obtaining Organic metal compound (XII). The synthesis pathway of the above reaction was as follows:
[0094] The physical measurement of Organic metal compound (XII) is listed below 1H NMR (500 MHz, CDCl3, 294 K): 8.37 (d, 2H), 7.90 (dd, 2H), 7.83 (s, 2H), 7.47 (s, 2H), 7.37 (d, 2H), 6.60 (dd, 2H), 5.87 (d, 2H), 5.25 (s, 1H), 1.80 (d, 6H).
Example 13: Preparation of Organic metal compound (XIII)
[0096] 1 mmol of Organic metal compound (XII), 2 mmol of Compound (XXX), and 15 mL of glycerol were added into a reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to 200 °C. After reacting for 48 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected and washed with water and ethyl acetate (EA), and then purified by column chromatography, obtaining Organic metal compound (XIII). The synthesis pathway of the above reaction was as follows:
[0097] The physical measurement of Organic metal compound (XIII) is listed below 1H NMR (500 MHz, CDCl3, 294 K): 8.00 (dd, 3H), 7.77 (d, 3H), 7.49 (d, 3H), 7.34 (d, 3H), 7.06 (d, 3H), 6.67 (dd, 3H), 6.53 (dd, 3H).
Example 14: Preparation of Organic metal compound (XIV)
[0099] 4.2 mmol of Compound (XXXII), 2 mmol of iridium trichloride (IrCl3), 15 ml of 2-methoxyethanol, and 5 ml of water were added into the reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to reflux. After reacting for 24 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected, washed with water and methanol, and dried, obtaining Compound (XXXIII). The synthesis pathway of the above reaction was as follows:
[0100] Next, 1 mmol of Compound (XXXIII), 3 mmol of acetylacetone, 2 mmol of sodium carbonate (Na2CO3), and 10 ml of 2-methoxyethanol were added into a reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to 120 °C. After reacting for 12 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected and washed with water and hexane, and then dissolved in dichloromethane. Next, the solution was extracted three times using dichloromethane and water. Next, an organic phase was separated and concentrated, and then purified by column chromatography, obtaining Organic metal compound (XIV). The synthesis pathway of the above reaction was as follows:
[0101] The physical measurement of Organic metal compound (XIII) is listed below 1H NMR (500 MHz, CDCl3, 294 K): 8.37 (d, 2H), 7.86 (d, 2H), 7.77 (s, 2H), 7.45 (s, 2H), 7.26 (d, 2H), 6.45 (d, 2H), 5.78 (s, 2H), 5.21 (s, 1H), 3.51 (s, 6H), 1.77 (s, 6H).
Example 15: Preparation of Organic metal compound (XV)
[0103] 1 mmol of Organic metal compound (XIV), 2 mmol of Compound (XXXII), and 15 mL of glycerol were added into a reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to 200 °C. After reacting for 48 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected and washed with water and ethyl acetate (EA), and then purified by column chromatography, obtaining Organic metal compound (XV). The synthesis pathway of the above reaction was as follows:
[0104] The physical measurement of Organic metal compound (XV) is listed below 1H NMR (500 MHz, CDCl3, 294 K): 7.94 (d, 3H), 7.70 (s, 3H), 7.46 (s, 3H), 7.33 (d, 3H), 6.97 (d, 3H), 6.51 (d, 6H), 3.55 (s, 9H).
Example 16: Preparation of Organic metal compound (XVI)
[0106] 4.2 mmol of Compound (XXXIV), 2 mmol of iridium trichloride (IrCl3), 15 ml of 2-methoxyethanol, and 5 ml of water were added into the reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to reflux. After reacting for 24 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected, washed with water and methanol, and dried, obtaining Compound (XXXV). The synthesis pathway of the above reaction was as follows:
[0107] Next, 1 mmol of Compound (XXXV), 3 mmol of acetylacetone, 2 mmol of sodium carbonate (Na2CO3), and 10 ml of 2-methoxyethanol were added into a reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to 120 °C. After reacting for 12 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected and washed with water and hexane, and then dissolved in dichloromethane. Next, the solution was extracted three times using dichloromethane and water. Next, an organic phase was separated and concentrated, and then purified by column chromatography, obtaining Organic metal compound (XVI). The synthesis pathway of the above reaction was as follows:
[0108] The physical measurement of Organic metal compound (XVI) is listed below 1H NMR (500 MHz, CDCl3, 294 K): 8.30 (d, 2H), 7.77 (d, 2H), 7.75 (s, 2H), 7.60 (d, 2H), 7.17 (d, 2H), 6.50 (s, 2H), 5.03 (s, 1H), 2.30 (s, 6H), 1.62 (s, 6H), 1.32 (s, 6H).
Example 17: Preparation of Organic metal compound (XVII)
[0110] 4.2 mmol of Compound (XXXVI), 2 mmol of iridium trichloride (IrCl3), 15 ml of 2-methoxyethanol, and 5 ml of water were added into the reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to reflux. After reacting for 24 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected, washed with water and methanol, and dried, obtaining Compound (XXXVII). The synthesis pathway of the above reaction was as follows:
[0111] Next, 1 mmol of Compound (XXXVII), 3 mmol of acetylacetone, 2 mmol of sodium carbonate (Na2CO3), and 10 ml of 2-methoxyethanol were added into a reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to 120 °C. After reacting for 12 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected and washed with water and hexane, and then dissolved in dichloromethane. Next, the solution was extracted three times using dichloromethane and water. Next, an organic phase was separated and concentrated, and then purified by column chromatography, obtaining Organic metal compound (XVII). The synthesis pathway of the above reaction was as follows:
[0112] The physical measurement of Organic metal compound (XVII) is listed below: 1H NMR (500 MHz, CDCl3, 294 K): 8.32 (d, 2H), 7.74 (d, 2H), 7.21 (d, 2H), 7.19 (s, 2H), 6.64 (d, 2H), 6.08 (s, 2H), 5.18 (s, 1H), 2.60 (s, 6H), 2.03 (s, 6H), 1.74 (s, 6H).
Example 18: Preparation of Organic metal compound (XVIII)
[0114] 4.2 mmol of Compound (XXXVIII), 2 mmol of iridium trichloride (IrCl3), 15 ml of 2-methoxyethanol, and 5 ml of water were added into the reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to reflux. After reacting for 24 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected, washed with water and methanol, and dried, obtaining Compound (XXXIX). The synthesis pathway of the above reaction was as follows:
[0115] Next, 1 mmol of Compound (XXXIX), 3 mmol of acetylacetone, 2 mmol of sodium carbonate (Na2CO3), and 10 ml of 2-methoxyethanol were added into a reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to 120 °C. After reacting for 12 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected and washed with water and hexane, and then dissolved in dichloromethane. Next, the solution was extracted three times using dichloromethane and water. Next, an organic phase was separated and concentrated, and then purified by column chromatography, obtaining Organic metal compound (XVIII). The synthesis pathway of the above reaction was as follows:
[0116] The physical measurement of Organic metal compound (XVIII) is listed below: 1H NMR (500 MHz, CDCl3, 294 K): 8.36 (d, 2H), 7.75 (d, 2H), 7.23 (d, 2H), 7.09 (s,2H), 6.86 (d, 2H), 6.23 (s, 2H), 5.19 (s, 1H), 2.61 (s, 6H), 1.76 (s, 6H), 1.00 (s, 18H).
Example 19: Preparation of Organic metal compound (XIX)
[0118] 1 mmol of Organic metal compound (XVIII), 2 mmol of Compound (XXXVIII), and 15 mL of glycerol were added into a reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to 200 °C. After reacting for 48 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected and washed with water and ethyl acetate (EA), and then purified by column chromatography, obtaining Organic metal compound (XIX). The synthesis pathway of the above reaction was as follows:
[0119] The physical measurement of Organic metal compound (XIX) is listed below: 1H NMR (500 MHz, CDCl3, 294 K): 7.93 (d, 3H), 7.20 (s, 3H), 7.08 (s, 3H), 6.82 (d, 3H), 6.77 (s, 3H), 6.57 (s, 3H), 2.55 (s, 9H), 1.10 (s, 27H).
Example 20: Preparation of Organic metal compound (XX)
[0121] 1 mmol of Compound (XIV) and 10 mL of dichloromethane were added into a first reaction bottle. 2.2 mmol of silver trifluoromethanesulfonate (AgOTf) and 5 mL of methanol were added into a second reaction bottle, obtaining a methanol solution. Next, the methanol solution was added into the first reaction bottle, and the mixture was stirred for 18 hr. Next, after filtrating for removing sliver chloride and concentrating, Compound (XL) is obtained. The synthesis pathway of the above reaction was as follows:
[0122] Next, 1 mmol of Compound (XL), 2.5 mmol of Compound (XLI), 5 ml of methanol, and 5 ml of ethanol were added into a reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to 90 °C. After reacting for 12 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected and washed with water and hexane, and then dissolved in dichloromethane. Next, the solution was extracted three times using dichloromethane and water. Next, an organic phase was separated and concentrated, and then purified by column chromatography, obtaining Organic metal compound (XX). The synthesis pathway of the above reaction was as follows:
[0123] The physical measurement of Organic metal compound (XX) is listed below: 1H NMR (500 MHz, CDCl3, 294 K): 7.94 (t, 2H), 7.87 (d, 1H), 7.68∼7.65 (m, 3H), 7.56 (t, 1H), 7.54∼7.46 (m, 3H), 7.41 (d, 1H), 7.35 (d, 1H), 7.02 (d, 1H), 6.98∼6.83 (m, 7H), 6.82 (s, 1H), 1.12 (s, 9H), 1.08 (s, 9H).
Example 21: Preparation of Organic metal compound (XXI)
[0125] 4.2 mmol of Compound (XLI), 2 mmol of iridium trichloride (IrCl3), 15 ml of 2-methoxyethanol, and 5 ml of water were added into the reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to reflux. After reacting for 24 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected, washed with water and methanol, and dried, obtaining Compound (XLII). The synthesis pathway of the above reaction was as follows:
[0126] 1 mmol of Compound (XLII) and 10 mL of dichloromethane were added into a first reaction bottle. 2.2 mmol of silver trifluoromethanesulfonate (AgOTf) and 5 mL of methanol were added into a second reaction bottle, obtaining a methanol solution. Next, the methanol solution was added into the first reaction bottle, and the mixture was stirred for 18 hr. Next, after filtrating for removing sliver chloride and concentrating, Compound (XLIII) is obtained. The synthesis pathway of the above reaction was as follows:
[0127] Next, 1 mmol of Compound (XLIII), 2.5 mmol of Compound (V), 5 ml of methanol, and 5 ml of ethanol were added into a reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to 90 °C. After reacting for 12 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected and washed with water and hexane, and then dissolved in dichloromethane. Next, the solution was extracted three times using dichloromethane and water. Next, an organic phase was separated and concentrated, and then purified by column chromatography, obtaining Organic metal compound (XXI). The synthesis pathway of the above reaction was as follows:
[0128] The physical measurement of Organic metal compound (XXI) is listed below: 1H NMR (500 MHz, CDCl3, 294 K): 7.92 (d, 1H), 7.86 (d, 2H), 7.69 (s, 1H), 7.66 (d, 2H), 7.58∼7.56 (m, 2H), 7.50 (m, 2H), 7.45 (d, 1H), 7.38 (d, 1H), 7.01 (d, 1H), 6.90∼6.80 (m, 8H), 6.77 (d, 1H), 6.72 (s, 1H), 2.15 (s, 3H).
Example 22: Preparation of Organic metal compound (XXII)
[0130] 1 mmol of Compound (XLIII), 2.5 mmol of Compound (XIII), 5 ml of methanol, and 5 ml of ethanol were added into a reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to 90 °C. After reacting for 12 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected and washed with water and hexane, and then dissolved in dichloromethane. Next, the solution was extracted three times using dichloromethane and water. Next, an organic phase was separated and concentrated, and then purified by column chromatography, obtaining Organic metal compound (XXII). The synthesis pathway of the above reaction was as follows:
[0131] The physical measurement of Organic metal compound (XXII) is listed below: 1H NMR (500 MHz, Acetone-d6, 294 K): 8.09∼8.02 (m, 4H), 7.78∼7.71 (m, 5H), 7.67 (d, 1H), 7.64 (d, 1H), 7.55 (d, 1H), 7.27 (d, 1H), 7.06 (t, 1H), 7.00 (t, 1H), 6.97 (d, 1H), 6.92 (dd, 1H), 6.87 (d, 1H), 6.83∼6.80 (m, 2H), 6.77 (t, 1H), 6.72 (t, 1H), 6.66 (t, 1H), 1.03 (s, 9H).
Example 23: Preparation of Organic metal compound (XXIII)
[0133] 1 mmol of Compound (XLIII), 2.5 mmol of Compound (XXXVIII), 5 ml of methanol, and 5 ml of ethanol were added into a reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to 90 °C. After reacting for 12 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected and washed with water and hexane, and then dissolved in dichloromethane. Next, the solution was extracted three times using dichloromethane and water. Next, an organic phase was separated and concentrated, and then purified by column chromatography, obtaining Organic metal compound (XXIII). The synthesis pathway of the above reaction was as follows:
[0134] The physical measurement of Organic metal compound (XXIII) is listed below: 1H NMR (500 MHz, CDCl3, 294 K): 7.92∼7.85 (m, 3H), 7.67 (t, 2H), 7.59∼7.50 (m, 3H), 7.43 (s, 1H), 7.28 (s, 1H), 7.09 (s, 1H), 6.88∼6.62 (m, 11H), 2.54 (s, 3H), 1.09 (s, 9H).
Example 24: Preparation of Organic metal compound (XXIV)
[0136] 1 mmol of Compound (XLIII), 2.5 mmol of Compound (XXXVI), 5 ml of methanol, and 5 ml of ethanol were added into a reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to 90 °C. After reacting for 12 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected and washed with water and hexane, and then dissolved in dichloromethane. Next, the solution was extracted three times using dichloromethane and water. Next, an organic phase was separated and concentrated, and then purified by column chromatography, obtaining Organic metal compound (XXIV). The synthesis pathway of the above reaction was as follows:
[0137] The physical measurement of Organic metal compound (XXIV) is listed below: 1H NMR (500 MHz, Acetone-d6, 294 K): 8.07 (d, 2H), 7.95 (d, 1H), 7.76∼7.70 (m, 4H), 7.61 (d, 1H), 7.58 (d, 1H), 7.45 (d, 1H), 7.37 (s, 1H), 7.16 (d, 1H), 7.08 (dd, 1H), 7.00 (dd, 1H), 6.86∼6.76 (m, 4H), 6.73 (s, 1H), 6.70∼6.65 (m, 3H), 2.56 (s, 3H), 2.02 (s, 3H.
Example 25: Preparation of Organic metal compound (XXV)
[0139] 1 mmol of Compound (XLIII), 2.5 mmol of Compound (XLII), 5 ml of methanol, and 5 ml of ethanol were added into a reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to 90 °C. After reacting for 12 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected and washed with water and hexane, and then dissolved in dichloromethane. Next, the solution was extracted three times using dichloromethane and water. Next, an organic phase was separated and concentrated, and then purified by column chromatography, obtaining Organic metal compound (XXV). The synthesis pathway of the above reaction was as follows:
[0140] The physical measurement of Organic metal compound (XXV) is listed below: 1H NMR (500 MHz, Acetone-d6, 294 K): 8.08∼8.05 (m, 3H), 7.77∼7.71 (m, 4H), 7.65 (d, 1H), 7.59 (d, 1H), 7.50 (d, 1H), 7.42 (s, 1H), 7.20 (d, 1H), 7.66 (dd, 1H), 7.00 (dd, 1H), 6.89∼6.76 (m, 6H), 6.71∼6.65 (m, 3H).
Example 26: Preparation of Organic metal compound (XXVI)
[0142] 1 mmol of Compound (XLIII), 2.5 mmol of Compound (XVII), 5 ml of methanol, and 5 ml of ethanol were added into a reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to 90 °C. After reacting for 12 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected and washed with water and hexane, and then dissolved in dichloromethane. Next, the solution was extracted three times using dichloromethane and water. Next, an organic phase was separated and concentrated, and then purified by column chromatography, obtaining Organic metal compound (XXVI). The synthesis pathway of the above reaction was as follows:
[0143] The physical measurement of Organic metal compound (XXVI) is listed below: 1H NMR (500 MHz, Acetone-d6, 294 K): 8.15 (d, 1H), 8.09∼8.07 (m, 3H), 7.80 (s, 1H), 7.76∼7.71 (m, 4H), 7.65 (d, 1H), 7.60 (d, 1H), 7.58(d, 1H), 7.32 (d, 1H), 7.06 (dd, 1H), 7.00 (dd, 1H), 6.91∼6.87 (m, 2H), 6.82∼6.77 (m,4 H), 6.72∼6.66 (m, 3H).
Example 27: Preparation of Organic metal compound (XXVII)
[0145] 1 mmol of Compound (XLIII), 2.5 mmol of Compound (IX), 5 ml of methanol, and 5 ml of ethanol were added into a reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to 90 °C. After reacting for 12 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected and washed with water and hexane, and then dissolved in dichloromethane. Next, the solution was extracted three times using dichloromethane and water. Next, an organic phase was separated and concentrated, and then purified by column chromatography, obtaining Organic metal compound (XXVII). The synthesis pathway of the above reaction was as follows:
[0146] The physical measurement of Organic metal compound (XXVII) is listed below: 1H NMR (500 MHz, Acetone-d6, 294 K): 8.11 (t, 2H), 8.01 (d, 1H), 7.82∼7.73 (m, 4H), 7.68 (d, 1H), 7.60 (d, 1H), 7.56 (d, 1H), 7.47∼7.46 (m, 1H), 7.39 (d, 1H), 7.08∼7.04 (m, 2H), 6.86∼6.81 (m, 2H), 6.76∼6.71 (m, 4H), 6.48∼6.41 (m, 2H).
Example 28: Preparation of Organic metal compound (XXVIII)
[0148] 1 mmol of Compound (XLIII), 2.5 mmol of Compound (XXVI), 5 ml of methanol, and 5 ml of ethanol were added into a reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to 90 °C. After reacting for 12 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected and washed with water and hexane, and then dissolved in dichloromethane. Next, the solution was extracted three times using dichloromethane and water. Next, an organic phase was separated and concentrated, and then purified by column chromatography, obtaining Organic metal compound (XXVIII). The synthesis pathway of the above reaction was as follows:
[0149] The physical measurement of Organic metal compound (XXVIII) is listed below: 1H NMR (500 MHz, Acetone-d6, 294 K): 8.11 (t, 2H), 7.82∼7.73 (m, 4H), 7.60 (d, 2H), 7.54 (d, 1H), 7.29 (d, 1H), 7.09∼7.04 (m, 3H), 6.86∼6.81 (m, 2H), 6.76∼6.71 (m, 4H), 6.46∼6.40 (m, 2H), 2.54 (s, 3H).
Example 29: Preparation of Organic metal compound (XXIX)
[0151] 1 mmol of Compound (XLIII), 2.5 mmol of Compound (XXX), 5 ml of methanol, and 5 ml of ethanol were added into a reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to 90 °C. After reacting for 12 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected and washed with water and hexane, and then dissolved in dichloromethane. Next, the solution was extracted three times using dichloromethane and water. Next, an organic phase was separated and concentrated, and then purified by column chromatography, obtaining Organic metal compound (XXIX). The synthesis pathway of the above reaction was as follows:
[0152] The physical measurement of Organic metal compound (XXIX) is listed below: 1H NMR (500 MHz, Acetone-d6, 294 K): 8.20 (dd, 1H), 8.11∼8.06 (m, 3H), 7.79∼7.73 (m, 5H), 7.65 (d, 1H), 7.63 (d, 1H), 7.58 (d, 1H), 7.32 (d, 1H), 7.09∼7.02 (m, 2H), 6.84∼6.76 (m, 4H), 6.74∼6.71 (m, 2H), 6.62 (dd, 1H), 6.53 (dd, 1H).
Example 30: Preparation of Organic metal compound (XXX)
[0154] 1 mmol of Compound (XLIII), 2.5 mmol of Compound (XXXII), 5 ml of methanol, and 5 ml of ethanol were added into a reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to 90 °C. After reacting for 12 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected and washed with water and hexane, and then dissolved in dichloromethane. Next, the solution was extracted three times using dichloromethane and water. Next, an organic phase was separated and concentrated, and then purified by column chromatography, obtaining Organic metal compound (XXX). The synthesis pathway of the above reaction was as follows:
[0155] The physical measurement of Organic metal compound (XXX) is listed below: 1H NMR (500 MHz, Acetone-d6, 294 K): 8.10 ∼8.07 (m, 3H), 8.05 (d, 1H), 7.78∼7.71 (m, 5H), 7.66∼7.63 (m, 2H), 7.51 (d, 1H), 7.21 (d, 1H), 7.07∼7.00 (m, 2H), 6.88 (d, 1H), 6.84∼6.77 (m, 3H), 6.72∼6.68 (m, 2H), 6.49 (dd, 1H), 6.43 (d, 1H), 3.48 (s, 3H).
Example 31: Preparation of Organic metal compound (XXXI)
[0157] 1 mmol of Compound (XLIII), 2.5 mmol of Compound (XXI), 5 ml of methanol, and 5 ml of ethanol were added into a reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to 90 °C. After reacting for 12 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected and washed with water and hexane, and then dissolved in dichloromethane. Next, the solution was extracted three times using dichloromethane and water. Next, an organic phase was separated and concentrated, and then purified by column chromatography, obtaining Organic metal compound (XXXI). The synthesis pathway of the above reaction was as follows:
[0158] The physical measurement of Organic metal compound (XXXI) is listed below: 1H NMR (500 MHz, Acetone-d6, 294 K): 8.75(s, 1H), 8.18 (d, 1H), 8.11∼8.07 (m, 3H), 7.90 (d, 1H), 7.79∼7.67 (m, 7H), 7.40 (d, 1H), 7.20∼7.14 (m, 4H), 7.07 (dd, 1H), 6.97 (dd, 1H), 6.88∼6.73 (m, 5H), 6.61 (dd, 1H).
Example 32: Preparation of Organic metal compound (XXXII)
[0160] 4.2 mmol of Compound (XLIV), 2 mmol of iridium trichloride (IrCl3), 15 ml of 2-methoxyethanol, and 5 ml of water were added into the reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to reflux. After reacting for 24 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected, washed with water and methanol, and dried, obtaining Compound (XLV). The synthesis pathway of the above reaction was as follows:
[0161] 1 mmol of Compound (XLV) and 10 mL of dichloromethane were added into a first reaction bottle. 2.2 mmol of silver trifluoromethanesulfonate (AgOTf) and 5 mL of methanol were added into a second reaction bottle, obtaining a methanol solution. Next, the methanol solution was added into the first reaction bottle, and the mixture was stirred for 18 hr. Next, after filtrating for removing sliver chloride and concentrating, Compound (XLVI) is obtained. The synthesis pathway of the above reaction was as follows:
[0162] Next, 1 mmol of Compound (XLVI), 2.5 mmol of Compound (V), 5 ml of methanol, and 5 ml of ethanol were added into a reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to 90 °C. After reacting for 12 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected and washed with water and hexane, and then dissolved in dichloromethane. Next, the solution was extracted three times using dichloromethane and water. Next, an organic phase was separated and concentrated, and then purified by column chromatography, obtaining Organic metal compound (XXXII). The synthesis pathway of the above reaction was as follows:
[0163] The physical measurement of Organic metal compound (XXXII) is listed below: 1H NMR (500 MHz, CDCl3, 294 K): 7.87 (d, 1H), 7.83 (d, 1H), 7.80 (d, 1H), 7.71 (d, 1H), 7.66 (d, 1H), 7.62 (d, 1H), 7.58 (d, 1H), 7.53 (t, 1H), 7.46∼7.42 (m, 2H), 6.95 (d, 1H), 6.91∼6.86 (m, 2H), 6.81∼6.63 (m, 5H), 6.55 (d, 1H), 6.48∼6.45 (m, 2H), 2.07 (s, 3H), 2.00 (s, 3H), 1.87 (s, 3H).
Example 33: Preparation of Organic metal compound (XXXIII)
[0165] Next, 1 mmol of Compound (XLVI), 2.5 mmol of Compound (XIII), 5 ml of methanol, and 5 ml of ethanol were added into a reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to 90 °C. After reacting for 12 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected and washed with water and hexane, and then dissolved in dichloromethane. Next, the solution was extracted three times using dichloromethane and water. Next, an organic phase was separated and concentrated, and then purified by column chromatography, obtaining Organic metal compound (XXXIII). The synthesis pathway of the above reaction was as follows:
[0166] The physical measurement of Organic metal compound (XXXIII) is listed below: 1H NMR (500 MHz, CDCl3, 294 K): 7.86∼7.81 (m, 3H), 7.73 (d, 1H), 7.65 (d, 1H), 7.60∼7.54 (m, 3H), 7.44∼7.38 (m, 2H), 6.95∼6.88 (m, 4H), 6.80 (t, 1H), 6.73 (t, 1H), 6.68∼6.59 (m, 4H), 6.47 (d, 1H), 2.04 (s, 3H), 1.86 (s, 3H), 1.02 (s, 9H).
Example 34: Preparation of Organic metal compound (XXXIV)
[0168] Next, 1 mmol of Compound (XLVI), 2.5 mmol of Compound (XXXVIII), 5 ml of methanol, and 5 ml of ethanol were added into a reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to 90 °C. After reacting for 12 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected and washed with water and hexane, and then dissolved in dichloromethane. Next, the solution was extracted three times using dichloromethane and water. Next, an organic phase was separated and concentrated, and then purified by column chromatography, obtaining Organic metal compound (XXXIV). The synthesis pathway of the above reaction was as follows:
[0169] The physical measurement of Organic metal compound (XXXIV) is listed below: 1H NMR (500 MHz, CDCl3, 294 K): 8.00 (dd, 2H), 7.90 (d, 1H), 7.80 (d, 1H), 7.73∼7.65 (m, 3H), 7.56 (t, 1H), 7.32 (s, 1H), 7.08∼7.05 (m, 2H), 6.88 (dd, 1H), 6.84∼6.81 (m, 2H), 6.73∼6.69 (m, 2H), 6.60∼6.59 (m, 2H), 6.50∼6.45 (m, 2H), 2.53 (s, 3H), 2.05 (s, 3H), 1.93 (s, 3H), 0.99 (s, 9H).
Example 35: Preparation of Organic metal compound (XXXV)
[0171] Next, 1 mmol of Compound (XLVI), 2.5 mmol of Compound (XXXVI), 5 ml of methanol, and 5 ml of ethanol were added into a reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to 90 °C. After reacting for 12 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected and washed with water and hexane, and then dissolved in dichloromethane. Next, the solution was extracted three times using dichloromethane and water. Next, an organic phase was separated and concentrated, and then purified by column chromatography, obtaining Organic metal compound (XXXV). The synthesis pathway of the above reaction was as follows:
[0172] The physical measurement of Organic metal compound (XXXV) is listed below: 1H NMR (500 MHz, CDCl3, 294 K): 7.85∼7.79 (m, 3H), 7.76 (d, 1H), 7.60 (d, 1H), 7.52 (dd, 2H), 7.44 (dd, 1H), 7.07(s, 1H), 6.83∼6.63 (m, 8H), 6.43 (s, 1H), 6.36 (s, 2H), 2.50 (s, 3H), 2.05 (s, 3H), 1.96 (s, 3H), 1.86 (s, 3H).
Example 36: Preparation of Organic metal compound (XXXVI)
[0174] Next, 1 mmol of Compound (XLVI), 2.5 mmol of Compound (XLII), 5 ml of methanol, and 5 ml of ethanol were added into a reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to 90 °C. After reacting for 12 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected and washed with water and hexane, and then dissolved in dichloromethane. Next, the solution was extracted three times using dichloromethane and water. Next, an organic phase was separated and concentrated, and then purified by column chromatography, obtaining Organic metal compound (XXXVI). The synthesis pathway of the above reaction was as follows:
[0175] The physical measurement of Organic metal compound (XXXVI) is listed below: 1H NMR (500 MHz, CDCl3, 294 K): 7.94 (d, 1H), 7.81 (dd, 2H), 7.74 (s, 1H), 7.59∼7.52 (m, 3H), 7.44 (dd, 1H), 7.09(s, 1H), 6.93∼6.77 (m, 7H), 6.67 (d, 1H), 6.63 (dd, 1H), 6.60 (s, 1H), 6.49 (s, 1H), 6.35 (s, 1H), 2.51 (s, 3H), 1.99 (s, 3H), 1.86 (s, 3H).
Example 37: Preparation of Organic metal compound (XXXVII)
[0177] Next, 1 mmol of Compound (XLVI), 2.5 mmol of Compound (XVII), 5 ml of methanol, and 5 ml of ethanol were added into a reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to 90 °C. After reacting for 12 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected and washed with water and hexane, and then dissolved in dichloromethane. Next, the solution was extracted three times using dichloromethane and water. Next, an organic phase was separated and concentrated, and then purified by column chromatography, obtaining Organic metal compound (XXXVII). The synthesis pathway of the above reaction was as follows:
[0178] The physical measurement of Organic metal compound (XXXVII) is listed below: 1H NMR (500 MHz, CDCl3, 294 K): 7.99 (d, 1H), 7.82 (dd, 2H), 7.74 (d, 1H), 7.69 (s, 1H), 7.65 (s, 1H), 7.59 (s, 1H), 7.54 (dd, 1H), 7.49 (s, 1H), 7.44 (dd, 1H), 6.99 (d, 1H), 6.94 (dd, 1H), 6.87∼6.85 (m, 2H), 6.80∼6.74 (m, 3H), 6.68 (d, 1H), 6.63 (dd, 2H), 6.49 (s, 1H), 6.37 (s, 1H), 2.00 (s, 3H), 1.86 (s, 3H).
Example 38: Preparation of Organic metal compound (XXXVIII)
[0180] Next, 1 mmol of Compound (XLVI), 2.5 mmol of Compound (IX), 5 ml of methanol, and 5 ml of ethanol were added into a reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to 90 °C. After reacting for 12 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected and washed with water and hexane, and then dissolved in dichloromethane. Next, the solution was extracted three times using dichloromethane and water. Next, an organic phase was separated and concentrated, and then purified by column chromatography, obtaining Organic metal compound (XXXVIII). The synthesis pathway of the above reaction was as follows:
[0181] The physical measurement of Organic metal compound (XXXVIII) is listed below: 1H NMR (500 MHz, CDCl3, 294 K): 7.85 (d, 1H), 7.80 (d, 1H), 7.73 (d, 1H), 7.71 (d, 1H), 7.60 (d, 1H), 7.56∼7.47 (m, 3H), 7.40 (s, 1H), 7.02 (d, 1H), 6.90∼6.87 (m, 2H), 6.82 (t, 1H), 6.75 (d, 1H), 6.72 (t, 1H), 6.66 (t, 1H), 6.47 (d, 2H), 6.38 (ddd, 1H), 6.15 (dd, 1H), 1.99 (s, 3H), 1.94 (s, 3H).
Example 39: Preparation of Organic metal compound (XXXIX)
[0183] Next, 1 mmol of Compound (XLVI), 2.5 mmol of Compound (XXVI), 5 ml of methanol, and 5 ml of ethanol were added into a reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to 90 °C. After reacting for 12 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected and washed with water and hexane, and then dissolved in dichloromethane. Next, the solution was extracted three times using dichloromethane and water. Next, an organic phase was separated and concentrated, and then purified by column chromatography, obtaining Organic metal compound (XXXIX). The synthesis pathway of the above reaction was as follows:
[0184] The physical measurement of Organic metal compound (XXXIX) is listed below: 1H NMR (500 MHz, CDCl3, 294 K): 7.85 (d, 1H), 7.79 (d, 1H), 7.70 (d, 1H), 7.66 (d, 1H), 7.56∼7.47 (m, 3H), 6.99 (d, 1H), 6.92∼6.86 (m, 3H), 6.813 (t, 1H), 6.76∼6.70 (m, 2H), 6.66 (t, 1H), 6.48 (d, 2H), 6.36 (ddd, 1H), 6.13 (dd, 1H), 2.54 (s, 3H), 1.99 (s, 3H), 1.94 (s, 3H).
Example 40: Preparation of Organic metal compound (XL)
[0186] Next, 1 mmol of Compound (XLVI), 2.5 mmol of Compound (XXX), 5 ml of methanol, and 5 ml of ethanol were added into a reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to 90 °C. After reacting for 12 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected and washed with water and hexane, and then dissolved in dichloromethane. Next, the solution was extracted three times using dichloromethane and water. Next, an organic phase was separated and concentrated, and then purified by column chromatography, obtaining Organic metal compound (XL). The synthesis pathway of the above reaction was as follows:
[0187] The physical measurement of Organic metal compound (XL) is listed below: 1H NMR (500 MHz, CDCl3, 294 K): 7.95 (dd, 1H), 7.86 (d, 1H), 7.81 (d, 1H), 7.72 (d, 1H), 7.69 (s, 1H), 7.62 (d, 1H), 7.58∼7.53 (m, 2H), 7.47 (dd, 1H), 7.42 (s, 1H), 7.00 (d, 1H), 6.92∼6.88 (m, 2H), 6.81 (dd, 1H), 6.75∼6.71 (m, 2H), 6.67∼6.62 (m, 2H), 6.53 (d, 1H), 6.43 (d, 1H), 6.31 (dd, 1H), 2.00 (s, 3H), 1.85 (s, 3H).
Example 41: Preparation of Organic metal compound (XLI)
[0189] Next, 1 mmol of Compound (XLVI), 2.5 mmol of Compound (XXXII), 5 ml of methanol, and 5 ml of ethanol were added into a reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to 90 °C. After reacting for 12 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected and washed with water and hexane, and then dissolved in dichloromethane. Next, the solution was extracted three times using dichloromethane and water. Next, an organic phase was separated and concentrated, and then purified by column chromatography, obtaining Organic metal compound (XLI). The synthesis pathway of the above reaction was as follows:
[0190] The physical measurement of Organic metal compound (XLI) is listed below: 1H NMR (500 MHz, CDCl3, 294 K): 7.90 (d, 1H), 7.83 (d, 1H), 7.81 (d, 1H), 7.70 (d, 1H), 7.65 (s, 1H), 7.59∼7.52 (m, 3H), 7.46∼7.41 (m, 2H), 6.92 (d, 1H), 6.89∼6.86 (m, 2H), 6.81 (dd, 1H), 6.73∼6.70 (m, 2H), 6.65 (dd, 1H), 6.57 (d, 1H), 6.52∼6.47 (m, 2H), 6.19 (d, 1H), 3.47 (s, 3H), 2.00 (s, 3H), 1.88 (s, 3H).
Example 42: Preparation of Organic metal compound (XLII)
[0192] Next, 1 mmol of Compound (XLVI), 2.5 mmol of Compound (XXI), 5 ml of methanol, and 5 ml of ethanol were added into a reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to 90 °C. After reacting for 12 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected and washed with water and hexane, and then dissolved in dichloromethane. Next, the solution was extracted three times using dichloromethane and water. Next, an organic phase was separated and concentrated, and then purified by column chromatography, obtaining Organic metal compound (XLII). The synthesis pathway of the above reaction was as follows:
[0193] The physical measurement of Organic metal compound (XLII) is listed below: 1H NMR (500 MHz, CDCl3, 294 K): 8.48 (s, 1H), 7.84 (d, 1H), 7.82 (d, 1H), 7.77∼7.73 (m, 4H), 7.70 (s, 1H), 7.58 (d, 1H), 7.55 (dd, 1H), 7.39 (dd, 1H), 7.32 (d, 1H), 7.21∼7.18 (m, 2H), 7.05 (d, 1H), 6.97 (s, 1H), 6.94 (dd, 1H), 6.89 (d, 1H), 6.80∼6.75 (m, 2H), 6.64 (d, 1H), 6.60 (d, 1H), 6.55 (dd, 1H), 6.47 (d, 1H), 2.03 (s, 3H), 1.88 (s, 3H).
Example 43: Preparation of Organic metal compound (XLIII)
[0195] Next, 1 mmol of Compound (XLVII), 2.5 mmol of Compound (XIII), 5 ml of methanol, and 5 ml of ethanol were added into a reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to 90 °C. After reacting for 12 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected and washed with water and hexane, and then dissolved in dichloromethane. Next, the solution was extracted three times using dichloromethane and water. Next, an organic phase was separated and concentrated, and then purified by column chromatography, obtaining Organic metal compound (XLIII). The synthesis pathway of the above reaction was as follows:
[0196] The physical measurement of Organic metal compound (XLIII) is listed below: 1H-NMR (500 MHz, CDCl3, 294 K): 8.99∼8.93 (m, 2H), 8.11 (t, 2H), 7.95 (d, 1H), 7.74∼7.69 (m, 3H), 7.63∼7.59 (m, 4H), 7.51 (s, 1H), 7.35 (d, 1H), 7.24 (d, 1H), 7.20 (d, 1H), 7.12∼7.07(m, 3H), 7.03∼6.95 (m, 5H), 6.82 (s, 1H), 1.14 (s, 9H), 1.12 (s, 9H), 1.09 (s, 9H).
Example 44: Preparation of Organic metal compound (XLIV)
[0198] Next, 1 mmol of Compound (XLVII), 2.5 mmol of Compound (XXXVIII), 5 ml of methanol, and 5 ml of ethanol were added into a reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to 90 °C. After reacting for 12 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected and washed with water and hexane, and then dissolved in dichloromethane. Next, the solution was extracted three times using dichloromethane and water. Next, an organic phase was separated and concentrated, and then purified by column chromatography, obtaining Organic metal compound (XLIV). The synthesis pathway of the above reaction was as follows:
[0199] The physical measurement of Organic metal compound (XLIV) is listed below: 1H NMR (500 MHz, CDCl3, 294 K): 8.98∼8.93 (m, 2H), 8.12∼8.08 (t, 2H), 7.88 (d, 1H), 7.73∼6.69 (m, 2H), 7.63∼7.57 (m, 4H), 7.34 (d, 1H), 7.24 (d, 1H), 7.13∼6.92 (m, 9H), 6.84 (d, 1H), 6.80 (s, 1H), 2.52 (s, 3H), 1.14 (s, 9H), 1.12 (s, 9H), 1.08 (s, 9H).
Example 45: Preparation of Organic metal compound (XLV)
[0201] Next, 1 mmol of Compound (XLVIII), 2.5 mmol of Compound (XIII), 5 ml of methanol, and 5 ml of ethanol were added into a reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to 90 °C. After reacting for 12 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected and washed with water and hexane, and then dissolved in dichloromethane. Next, the solution was extracted three times using dichloromethane and water. Next, an organic phase was separated and concentrated, and then purified by column chromatography, obtaining Organic metal compound (XLV). The synthesis pathway of the above reaction was as follows:
[0202] The physical measurement of Organic metal compound (XLV) is listed below: 1H NMR (500 MHz, CDCl3, 294 K): 8.91 (m, 2H), 8.04 (m, 2H), 7.92 (d, 2H), 7.69 (d, 2H), 7.60 (m, 2H), 7.49 (m, 2H), 7.38∼7.30 (m, 2H), 7.23∼7.16 (m, 3H), 7.08∼6.78 (m, 8H), 2.20 (s, 3H), 2.16 (s, 3H), 1.11 (s, 9H).
Example 46: Preparation of Organic metal compound (XLVI)
[0204] Next, 1 mmol of Compound (XLVIII), 2.5 mmol of Compound (XXXVIII), 5 ml of methanol, and 5 ml of ethanol were added into a reaction bottle. Next, after removing moisture and purging nitrogen gas several times, the reaction bottle was heated to 90 °C. After reacting for 12 hr and cooling down to room temperature, the result was filtrated. The filter cake was collected and washed with water and hexane, and then dissolved in dichloromethane. Next, the solution was extracted three times using dichloromethane and water. Next, an organic phase was separated and concentrated, and then purified by column chromatography, obtaining Organic metal compound (XLVI). The synthesis pathway of the above reaction was as follows:
[0205] The physical measurement of Organic metal compound (XLVI) is listed below: 1H NMR (500 MHz, CDCl3, 294 K): 8.92 (m, 1H), 8.05 (m, 1H), 7.86 (m, 2H), 7.73 (m, 1H), 7.60 (m, 2H), 7.37∼7.20 (m, 3H), 7.16∼7.12 (m, 4H), 6.98∼6.78 (m, 10H), 2.52 (s, 3H), 2.20 (s, 3H), 2.16 (s, 3H), 1.10 (s, 9H).
[0206] Due to the furopyridine derivative functional group, the organic metal compound having the structure of Formula (I) or Formula (II) of the disclosure can serve as a dapant of the light emitting layer, resulting in the organic light-emitting device employing the organic metal compound of the disclosure having increased electron conductivity, high luminous efficiency, and improved life-time.
[0207] In addition, since the reactants and reagents for synthesizing the compound having furopyridine derivative functional group are dangerous and the steps are complicated time-consuming, it is generally considered that the compound having furopyridine derivative functional group is difficult to be synthesized. As a result, few reports on the research and development of the compound having furopyridine derivative functional group. The disclosure provides an iridium complex having furopyridine functional group and a process for preparing the iridium complex having furopyridine derivative functional group with a relatively high yield.
[0208] The conventional blue phosphorescent material FIr(pic) (having a structure represented by
) has a sublimation yield of about 50%. On the other hand, due to the furopyridine derivative functional group bonded to Ir, the organic metal compound having a structure of Formula (I) or Formula (II) of the disclosure is suitable for being purified by a sublimation process (i.e. the organic metal compound having a structure of Formula (I) or Formula (II) of the disclosure has a sublimation yield that is greater than 80%).
[0209] The photoluminescence (PL) spectra of the organic metal compound having a structure of Formula (I) or Formula (II) of the disclosure as disclosed in Examples were measured, and the results were shown in Table 1.
Table 1
| organic metal compound | maximum PL wavelength (nm) |
| organic metal compound (I) | 532 |
| organic metal compound (II) | 504 |
| organic metal compound (VI) | 562 |
| organic metal compound (VII) | 501 |
| organic metal compound (XI) | 534 |
| organic metal compound (XII) | 497 |
| organic metal compound (XIII) | 562 |
| organic metal compound (XIV) | 520 |
| organic metal compound(XVI) | 561 |
| organic metal compound (XX) | 534 |
| organic metal compound (XXI) | 529 |
| organic metal compound (XXII) | 530 |
| organic metal compound (XXIII) | 520 |
| organic metal compound (XXIV) | 518 |
| organic metal compound (XXV) | 523 |
| organic metal compound (XXVI) | 532 |
| organic metal compound (XXVII) | 516 |
| organic metal compound (XXVIII) | 506 |
| organic metal compound (XXIX) | 516 |
| organic metal compound (XXX) | 516 |
| organic metal compound (XXXI) | 566 |
| organic metal compound (XXXII) | 529 |
| organic metal compound (XXXIII) | 529 |
| organic metal compound (XXXIV) | 522 |
| organic metal compound (XXXV) | 519 |
| organic metal compound (XXXVI) | 524 |
| organic metal compound (XXXVII) | 534 |
| organic metal compound (XXXVIII) | 518 |
| organic metal compound (XXXIX) | 508 |
| organic metal compound (XL) | 518 |
| organic metal compound (XLI) | 518 |
| organic metal compound (XLII) | 563 |
| organic metal compound (XLIII) | 620 |
Organic light-emitting device
[0210] Fig. 1 shows an embodiment of an organic light-emitting device 10. The organic light-emitting device 10 includes a substrate 12, a bottom electrode 14, an organic light-emitting element 16, and a top electrode 18, as shown in Fig. 1. The organic light-emitting device can be a top-emission, bottom-emission, or dual-emission devices. The substrate 12 can be a glass, plastic, or semiconductor substrate. Suitable materials for the bottom and top electrodes can be Ca, Ag, Mg, Al, Li, In, Au, Ni, W, Pt, Cu, indium tin oxide (ITO), indium zinc oxide (IZO), aluminum zinc oxide (AZO), or zinc oxide (ZnO), formed by sputtering, electron beam evaporation, thermal evaporation, or chemical vapor deposition. Furthermore, at least one of the bottom and top electrodes 14 and 18 is transparent.
[0211] The organic light-emitting element 16 at least includes an emission layer, and can further include a hole injection layer, a hole transport layer, an electron transport layer, and an electron injection layer. In an embodiment of the disclosure, at least one layer of the organic light-emitting element 16 includes the organic metal compound having a structure of Formula (I) of the disclosure.
[0212] According to another embodiment of the disclosure, the organic light-emitting device can be a phosphorescent organic light-emitting device, and the emission layer of the organic light-emitting element can include a host material and a dopant, wherein the dopant can include the organic metal compound having a structure of Formula (I) of the disclosure. The dose of the dopant is not limited and can be optionally modified by a person of ordinary skill in the field
[0213] In order to clearly disclose the organic light-emitting devices of the disclosure, the following examples (having an emitting layer employing the organic metal compounds of the disclosure formed by deposition (dry process) or coating (wet process)) are intended to illustrate the disclosure more fully without limiting their scope, since numerous modifications and variations will be apparent to those skilled in this art.
Example 47: Organic light-emitting device (I)
[0214] A glass substrate with an indium tin oxide (ITO) film with a thickness of 120 nm was provided and then washed with a cleaning agent, acetone, and isopropanol with ultrasonic agitation. After drying with nitrogen flow, the ITO film was subjected to a UV/ozone treatment for 30 min.
[0215] Next, PEDOT:PSS (Poly(3,4-ethylenedioxythiophene)-poly(styrenesulfonate)) was coated on the ITO film by a spin coating process (with a rotation rate of 800rpm for 3 sec and a rotation rate of 2000rpm for 40 sec) and baked at 130□ for 40 min to form a PEDOT:PSS film serving as a hole injection layer (with a thickness of 40nm). Next, TAPC (1,1-bis[4-[N,N'-di(p-tolyl)amino]phenyl]cyclobexane, with a thickness of 35nm), TCTA (4,4',4'-tri(N-carbazolyl)triphenylamine) doped with Organic metal compound (I) (the weight ratio between TCTA and Organic metal compound (I) was 94:6, with a thickness of 15nm), TmPyPB (1,3,5-tri(m-pyrid-3-yl-phenyl)benzene, with a thickness of 42nm), LiF (with a thickness of 0.5nm), and Al (with a thickness of 120nm), were subsequently formed on the PEDOT:PSS film at 10-6 torr, obtaining the organic light-emitting device (I) after encapsulation. The materials and layers formed therefrom are described in the following: ITO/PEDOT:PSS/TAPC/TCTA:organic metal compound (I)(6%)/TmPyPB/LiF/Al
[0216] Next, the optical properties (such as maximum emission peak, driving voltage, current efficiency, power efficiency, and C.I.E coordinate) of the light-emitting device (I) were measured by a spectra colorimeter PR650 (purchased from Photo Research Inc.) and a luminance meter LS110 (purchased from Konica Minolta). The results are shown in Table 2.
Example 48: organic light-emitting device (II)
[0217] Example 48 was performed in the same manner as in Example 47 except that Organic metal compound (II) was substituted for Organic metal compound (I), obtaining the organic light-emitting device (II). The materials and layers formed therefrom are described in the following: ITO/PEDOT:PSS /TAPC/TCTA:Organic metal compound (II) (6%)/TmPyPB /LiF/Al
[0218] Next, the optical properties (such as maximum emission peak, driving voltage, current efficiency, power efficiency, and C.I.E coordinate) of the light-emitting device (II) were measured by a spectra colorimeter PR650 (purchased from Photo Research Inc.) and a luminance meter LS110 (purchased from Konica Minolta). The results are shown in Table 2.
Comparative Example 1 : organic light-emitting device (III)
[0219] Comparative Example 1 was performed in the same manner as in Example 47 except that compound (R1) (having a structure of
) was substituted for Organic metal compound (I), obtaining the organic light-emitting device (III). The materials and layers formed therefrom are described in the following: ITO/PEDOT:PSS /TAPC/TCTA:compound (R1) (6%)/TmPyPB /LiF/Al
[0220] Next, the optical properties (such as maximum emission peak, driving voltage, current efficiency, power efficiency, and C.I.E coordinate) of the light-emitting device (III) were measured by a spectra colorimeter PR650 (purchased from Photo Research Inc.) and a luminance meter LS110 (purchased from Konica Minolta). The results are shown in Table 2.
Comparative Example 2: organic light-emitting device (IV)
[0221] Comparative Example 2 was performed in the same manner as in Example 47 except that compound (R2) (having a structure of
) was substituted for Organic metal compound (I), obtaining the organic light-emitting device (IV). The materials and layers formed therefrom are described in the following: ITO/PEDOT:PSS /TAPC/TCTA:compound (R2) (6%)/TmPyPB /LiF/Al
[0222] Next, the optical properties (such as maximum emission peak, driving voltage, current efficiency, power efficiency, and C.I.E coordinate) of the light-emitting device (IV) were measured by a spectra colorimeter PR650 (purchased from Photo Research Inc.) and a luminance meter LS110 (purchased from Konica Minolta). The results are shown in Table 2.
Comparative Example 3: organic light-emitting device (V)
[0223] Comparative Example 3 was performed in the same manner as in Example 47 except that Ir(ppy)3 (having a structure of
) was substituted for Organic metal compound (I), obtaining the organic light-emitting device (V). The materials and layers formed therefrom are described in the following: ITO/PEDOT:PSS /TAPC/TCTA: Ir(ppy)3 (6%)/TmPyPB /LiF/Al
[0224] Next, the optical properties (such as maximum emission peak, driving voltage, current efficiency, power efficiency, and C.I.E coordinate) of the light-emitting device (V) were measured by a spectra colorimeter PR650 (purchased from Photo Research Inc.) and a luminance meter LS110 (purchased from Konica Minolta). The results are shown in Table 2.
Table 2
| measured at a brightness of 1000 Cd/m2 | driving voltage (V) | measured at a brightness of 1000 Cd/m2 | |||
| current efficiency (cd/A) | power efficiency (lm/W) | C.I.E coordinate | maximum luminous intensity peak (nm) | ||
| organic light-emitting device (I) | 91.6 | 86.9 | 3.4 | (0.40,0.58) | 540 |
| organic light-emitting device (II) | 86.0 | 77.2 | 3.5 | (0.29,0.62) | 504 |
| organic light-emitting device (III) | 74 | 58.2 | 4.0 | (0.47,0.49) | 564 |
| organic light-emitting device (IV) | 48.9 | 34.2 | 4.5 | (0.39,0.58) | 528 |
| organic light-emitting device (V) | 56.3 | 36.8 | 4.8 | (0.31,0.62) | 516 |
[0225] As shown in Table 1, in comparison with the driving voltage of the organic light-emitting device (III) of Comparative Example 1, the organic light-emitting device (I) (employing the organic metal compound (I) as phosphorescent dopant) has a 0.6V decrease of driving voltage. Furthermore, the current efficiency of the organic light-emitting device (I) is about 1.2 times higher than that of the organic light-emitting device (III), and the power efficiency of the organic light-emitting device (I) is about 1.5 times higher than that of the organic light-emitting device (III).
Example 49: organic light-emitting device (VI)
[0226] A glass substrate with an indium tin oxide (ITO) film with a thickness of 120 nm was provided and then washed with a cleaning agent, acetone, and isopropanol with ultrasonic agitation. After drying with nitrogen flow, the ITO film was subjected to a UV/ozone treatment for 30 min.
[0227] Next, PEDOT:PSS (Poly(3,4-ethylenedioxythiophene)-poly(styrenesulfonate)) was coated on the ITO film by a spin coating process (with a rotation rate of 800rpm for 3 sec and a rotation rate of 2000rpm for 40 sec) and baked at 130□ for 40 min to form a PEDOT:PSS film serving as a hole injection layer (with a thickness of 40nm). Next, a composition was used for forming a light-emitting layer coated on the PEDOT:PSS film by a blade coating process and baked at 100°C for 40 min to form the light-emitting layer (with a thickness of 15nm). The composition used for forming a light-emitting layer includes TCTA (4,4',4'-tri(N-carbazolyl)triphenylamine) and Organic metal compound (I), wherein the weight ratio of TCTA and Organic metal compound (I) was 94:6, dissolved in chlorobenzene. Next, TmPyPB (1,3,5-tri(m-pyrid-3-yl-phenyl)benzene was coated on the light-emitting layer by a spin coating process to form a TmPyPB film (with a thickness of 50nm). Next, LiF (with a thickness of 1nm), and Al (with a thickness of 100nm) were subsequently formed on the TmPyPB film at 10-6 torr, obtaining the organic light-emitting device (VI) after encapsulation. The materials and layers formed therefrom are described in the following: ITO/PEDOT:PSS /TCTA: Organic metal compound (I) (6%)/TmPyPB/LiF/Al.
[0228] Next, the optical properties (such as maximum emission peak, driving voltage, current efficiency, power efficiency, and C.I.E coordinate) of the light-emitting device (VI) were measured by a spectra colorimeter PR650 (purchased from Photo Research Inc.) and a luminance meter LS110 (purchased from Konica Minolta). The results are shown in Table 3.
Example 50: organic light-emitting device (VII)
[0229] Example 50 was performed in the same manner as in Example 49 except that Organic metal compound (II) was substituted for Organic metal compound (I), obtaining the organic light-emitting device (VII). The materials and layers formed therefrom are described in the following: ITO/PEDOT:PSS/TCTA: Organic metal compound (II) (6%)/TmPyPB/LiF/Al.
[0230] Next, the optical properties (such as maximum emission peak, driving voltage, current efficiency, power efficiency, and C.I.E coordinate) of the light-emitting device (VII) were measured by a spectra colorimeter PR650 (purchased from Photo Research Inc.) and a luminance meter LS110 (purchased from Konica Minolta). The results are shown in Table 3.
Comparative Example 4: organic light-emitting device (VIII)
[0231] Comparative Example 4 was performed in the same manner as in Example 49 except that compound (R1) (having a structure of
) was substituted for Organic metal compound (I), obtaining the organic light-emitting device (VIII). The materials and layers formed therefrom are described in the following: ITO/PEDOT:PSS /TCTA: compound (R1) (6%)/TmPyPB/LiF/Al.
[0232] Next, the optical properties (such as maximum emission peak, driving voltage, current efficiency, power efficiency, and C.I.E coordinate) of the light-emitting device (VIII) were measured by a spectra colorimeter PR650 (purchased from Photo Research Inc.) and a luminance meter LS110 (purchased from Konica Minolta). The results are shown in Table 3.
Comparative Example 5: organic light-emitting device (IX)
[0233] Comparative Example 5 was performed in the same manner as in Example 49 except that compound (R2) (having a structure of
) was substituted for Organic metal compound (I), obtaining the organic light-emitting device (IX). The materials and layers formed therefrom are described in the following: ITO/PEDOT:PSS /TCTA: compound (R2) (6%)/TmPyPB/LiF/Al.
[0234] Next, the optical properties (such as maximum emission peak, driving voltage, current efficiency, power efficiency, and C.I.E coordinate) of the light-emitting device (IX) were measured by a spectra colorimeter PR650 (purchased from Photo Research Inc.) and a luminance meter LS110 (purchased from Konica Minolta). The results are shown in Table 3.
Table 3
| measured at a brightness of 1000 Cd/m2 | driving voltage (V) | measured at a brightness of 1000 Cd/m2 | |||
| current efficiency | power efficiency | C.I.E coordinate | maximum luminous | ||
| (cd/A) | (lm/W) | intensity peak (nm) | |||
| organic light-emitting device (VI) | 32.3 | 26.6 | 3.8 | (0.41,0.58) | 540 |
| organic light-emitting device (VII) | 39.6 | 36.5 | 3.4 | (0.29,0.62) | 504 |
| organic light-emitting device (VIII) | 26.7 | 21.0 | 4.0 | (0.49,0.51) | 560 |
| organic light-emitting device (IX) | 35 | 25.9 | 4.3 | (0.39,0.59) | 528 |
[0235] As shown in Table 3, in comparison with the driving voltage of the organic light-emitting device (VIII) of Comparative Example 4, the organic light-emitting device (VI) (employing the organic metal compound (VI) as phosphorescent dopant) has a 0.2V decrease of driving voltage. Furthermore, the current efficiency and power efficiency of the organic light-emitting device (I) is about 1.2 times higher than that of the organic light-emitting device (VIII). In addition, in comparison with the driving voltage of the organic light-emitting device (IX) of Comparative Example 5, the organic light-emitting device (VII) (employing the organic metal compound (II) as phosphorescent dopant) has a 0.9V decrease of driving voltage. Furthermore, the current efficiency of the organic light-emitting device (VII) is about 1.1 times higher than that of the organic light-emitting device (IX), and the power efficiency of the organic light-emitting device (VII) is about 1.4 times higher than that of the organic light-emitting device (IX).
Example 51: organic light-emitting device (X)
[0236] A glass substrate with an indium tin oxide (ITO) film with a thickness of 120 nm was provided and then washed with a cleaning agent, acetone, and isopropanol with ultrasonic agitation. After drying with nitrogen flow, the ITO film was subjected to a UV/ozone treatment for 30 min.
[0237] Next, PEDOT:PSS (Poly(3,4-ethylenedioxythiophene)-poly(styrenesulfonate)) was coated on the ITO film by a spin coating process (with a rotation rate of 800rpm for 3 sec and a rotation rate of 2000rpm for 40 sec) and baked at 130□ for 40 min to form a PEDOT:PSS film serving as a hole injection layer (with a thickness of 40nm). Next, TAPC (1,1-bis[4-[N,N'-di(p-tolyl)amino]phenyl]cyclobexane, with a thickness of 40nm), NPB (N,N'-bis(naphthalen-1-yl)-N,N'-bis(phenyl)-benzidine) doped with Organic metal compound (VI) (the weight ratio between TCTA and Organic metal compound (VI) was 97:3∼96:4, with a thickness of 15nm), TmPyPB (1,3,5-tri(m-pyrid-3-yl-phenyl)benzene, with a thickness of 50nm), LiF (with a thickness of 0.8nm), and Al (with a thickness of 120nm), were subsequently formed on the PEDOT:PSS film at 10-6 torr, obtaining the organic light-emitting device (X) after encapsulation. The materials and layers formed therefrom are described in the following: ITO/PEDOT:PSS/TAPC/NPB:organic metal compound (VI) (3∼4%)/TmPyPB/LiF/Al.
[0238] Next, the optical properties (such as maximum emission peak, driving voltage, current efficiency, power efficiency, and C.I.E coordinate) of the light-emitting device (X) were measured by a spectra colorimeter PR650 (purchased from Photo Research Inc.) and a luminance meter LS110 (purchased from Konica Minolta). The results are shown in Table 4.
Example 52: organic light-emitting device (XI)
[0239] A glass substrate with an indium tin oxide (ITO) film with a thickness of 120 nm was provided and then washed with a cleaning agent, acetone, and isopropanol with ultrasonic agitation. After drying with nitrogen flow, the ITO film was subjected to a UV/ozone treatment for 30 min.
[0240] Next, PEDOT:PSS (Poly(3,4-ethylenedioxythiophene)-poly(styrenesulfonate)) was coated on the ITO film by a spin coating process (with a rotation rate of 800rpm for 3 sec and a rotation rate of 2000rpm for 40 sec) and baked at 130□ for 40 min to form a PEDOT:PSS film serving as a hole injection layer (with a thickness of 40nm). Next, TAPC (1,1-bis[4-[N,N'-di(p-tolyl)amino]phenyl]cyclobexane, with a thickness of 40nm), TCTA(4,4',4'-tri(N-carbazolyl)triphenylamine) doped with Organic metal compound (VII) (the weight ratio between TCTA and Organic metal compound (VII) was 94:6∼92:8, with a thickness of 15nm), TmPyPB (1,3,5-tri(m-pyrid-3-yl-phenyl)benzene, with a thickness of 50nm), LiF (with a thickness of 0.8nm), and Al (with a thickness of 120nm), were subsequently formed on the PEDOT:PSS film at 10-6 torr, obtaining the organic light-emitting device (XI) after encapsulation. The materials and layers formed therefrom are described in the following: ITO/PEDOT:PSS/TAPC/TCTA:organic metal compound (VII) (6∼8%)/TmPyPB/LiF/Al.
[0241] Next, the optical properties (such as maximum emission peak, driving voltage, current efficiency, power efficiency, and C.I.E coordinate) of the light-emitting device (XI) were measured by a spectra colorimeter PR650 (purchased from Photo Research Inc.) and a luminance meter LS110 (purchased from Konica Minolta). The results are shown in Table 4.
Example 53: organic light-emitting device (XII)
[0242] A glass substrate with an indium tin oxide (ITO) film with a thickness of 120 nm was provided and then washed with a cleaning agent, acetone, and isopropanol with ultrasonic agitation. After drying with nitrogen flow, the ITO film was subjected to a UV/ozone treatment for 30 min.
[0243] Next, PEDOT:PSS (Poly(3,4-ethylenedioxythiophene)-poly(styrenesulfonate)) was coated on the ITO film by a spin coating process (with a rotation rate of 800rpm for 3 sec and a rotation rate of 2000rpm for 40 sec) and baked at 130□ for 40 min to form a PEDOT:PSS film serving as a hole injection layer (with a thickness of 40nm). Next, TAPC (1,1-bis[4-[N,N'-di(p-tolyl)amino]phenyl]cyclobexane, with a thickness of 40nm), NPB (N,N'-bis(naphthalen-1-yl)-N,N'-bis(phenyl)-benzidine) doped with Organic metal compound (VIII) (the weight ratio between NPB and Organic metal compound (VIII) was 95:5∼94:6, with a thickness of 15nm), TmPyPB (1,3,5-tri(m-pyrid-3-yl-phenyl)benzene, with a thickness of 50nm), LiF (with a thickness of 0.8nm), and Al (with a thickness of 120nm), were subsequently formed on the PEDOT:PSS film at 10-6 torr, obtaining the organic light-emitting device (XII) after encapsulation. The materials and layers formed therefrom are described in the following: ITO/PEDOT:PSS/NPB:organic metal compound (VIII) (5∼6%)/TmPyPB/LiF/Al.
[0244] Next, the optical properties (such as maximum emission peak, driving voltage, current efficiency, power efficiency, and C.I.E coordinate) of the light-emitting device (XII) were measured by a spectra colorimeter PR650 (purchased from Photo Research Inc.) and a luminance meter LS110 (purchased from Konica Minolta). The results are shown in Table 4.
Example 54: organic light-emitting device (XIII)
[0245] A glass substrate with an indium tin oxide (ITO) film with a thickness of 120 nm was provided and then washed with a cleaning agent, acetone, and isopropanol with ultrasonic agitation. After drying with nitrogen flow, the ITO film was subjected to a UV/ozone treatment for 30 min.
[0246] Next, PEDOT:PSS (Poly(3,4-ethylenedioxythiophene)-poly(styrenesulfonate)) was coated on the ITO film by a spin coating process (with a rotation rate of 800rpm for 3 sec and a rotation rate of 2000rpm for 40 sec) and baked at 130□ for 40 min to form a PEDOT:PSS film serving as a hole injection layer (with a thickness of 40nm). Next, TAPC (1,1-bis[4-[N,N'-di(p-tolyl)amino]phenyl]cyclobexane, with a thickness of 40nm), TCTA(4,4',4'-tri(N-carbazolyl)triphenylamine) doped with Organic metal compound (IX) (the weight ratio between TCTA and Organic metal compound (IX) was 94:6∼92:8, with a thickness of 15nm), TmPyPB (1,3,5-tri(m-pyrid-3-yl-phenyl)benzene, with a thickness of 50nm), LiF (with a thickness of 0.8nm), and Al (with a thickness of 120nm), were subsequently formed on the PEDOT:PSS film at 10-6 torr, obtaining the organic light-emitting device (XIII) after encapsulation. The materials and layers formed therefrom are described in the following: ITO/PEDOT:PSS/TAPC/TCTA:organic metal compound (IX) (6∼8%)/TmPyPB/LiF/Al.
[0247] Next, the optical properties (such as maximum emission peak, driving voltage, current efficiency, power efficiency, and C.I.E coordinate) of the light-emitting device (XIII) were measured by a spectra colorimeter PR650 (purchased from Photo Research Inc.) and a luminance meter LS110 (purchased from Konica Minolta). The results are shown in Table 4.
Example 55: organic light-emitting device (XIV)
[0248] Example 55 was performed in the same manner as in Example 47 except that Organic metal compound (XXIII) was substituted for Organic metal compound (I), obtaining the organic light-emitting device (XIV). The materials and layers formed therefrom are described in the following: ITO/PEDOT:PSS /TAPC/TCTA:Organic metal compound (XIV) (6-8%)/TmPyPB /LiF/Al
[0249] Next, the optical properties (such as maximum emission peak, driving voltage, current efficiency, power efficiency, and C.I.E coordinate) of the light-emitting device (XIV) were measured by a spectra colorimeter PR650 (purchased from Photo Research Inc.) and a luminance meter LS110 (purchased from Konica Minolta). The results are shown in Table 4.
Example 56: organic light-emitting device (XV)
[0250] Example 56 was performed in the same manner as in Example 47 except that Organic metal compound (XXVIII) was substituted for Organic metal compound (I), obtaining the organic light-emitting device (XV). The materials and layers formed therefrom are described in the following: ITO/PEDOT:PSS /TAPC/TCTA:Organic metal compound (XXVIII) (4-6%)/TmPyPB /LiF/Al
[0251] Next, the optical properties (such as maximum emission peak, driving voltage, current efficiency, power efficiency, and C.I.E coordinate) of the light-emitting device (XV) were measured by a spectra colorimeter PR650 (purchased from Photo Research Inc.) and a luminance meter LS110 (purchased from Konica Minolta). The results are shown in Table 4.
Example 57: organic light-emitting device (XVI)
[0252] Example 57 was performed in the same manner as in Example 47 except that Organic metal compound (XXXVII) was substituted for Organic metal compound (I), obtaining the organic light-emitting device (XVI). The materials and layers formed therefrom are described in the following: ITO/PEDOT:PSS /TAPC/TCTA:Organic metal compound (XXXVII) (6-8%)/TmPyPB /LiF/Al
[0253] Next, the optical properties (such as maximum emission peak, driving voltage, current efficiency, power efficiency, and C.I.E coordinate) of the light-emitting device (XVI) were measured by a spectra colorimeter PR650 (purchased from Photo Research Inc.) and a luminance meter LS110 (purchased from Konica Minolta). The results are shown in Table 4.
Example 58: organic light-emitting device (XVII)
[0254] Example 58 was performed in the same manner as in Example 47 except that Organic metal compound (XLII) was substituted for Organic metal compound (I), obtaining the organic light-emitting device (XVII). The materials and layers formed therefrom are described in the following: ITO/PEDOT:PSS /TAPC/TCTA:Organic metal compound (XLII) (2-6%)/TmPyPB /LiF/Al
[0255] Next, the optical properties (such as maximum emission peak, driving voltage, current efficiency, power efficiency, and C.I.E coordinate) of the light-emitting device (XVII) were measured by a spectra colorimeter PR650 (purchased from Photo Research Inc.) and a luminance meter LS110 (purchased from Konica Minolta). The results are shown in Table 4.
Example 59: organic light-emitting device (XVIII)
[0256] Example 59 was performed in the same manner as in Example 47 except that Organic metal compound (XLIII) was substituted for Organic metal compound (I), obtaining the organic light-emitting device (XVIII). The materials and layers formed therefrom are described in the following: ITO/PEDOT:PSS /TAPC/TCTA:Organic metal compound (XLIII) (2-4%)/TmPyPB /LiF/Al
[0257] Next, the optical properties (such as maximum emission peak, driving voltage, current efficiency, power efficiency, and C.I.E coordinate) of the light-emitting device (XVIII) were measured by a spectra colorimeter PR650 (purchased from Photo Research Inc.) and a luminance meter LS110 (purchased from Konica Minolta). The results are shown in Table 4.
Example 60: organic light-emitting device (XIX)
[0258] Example 60 was performed in the same manner as in Example 47 except that Organic metal compound (XX) was substituted for Organic metal compound (I), obtaining the organic light-emitting device (XIX). The materials and layers formed therefrom are described in the following: ITO/PEDOT:PSS /TAPC/TCTA:Organic metal compound (XX) (2-8%)/TmPyPB /LiF/Al
[0259] Next, the optical properties (such as maximum emission peak, driving voltage, current efficiency, power efficiency, and C.I.E coordinate) of the light-emitting device (XIX) were measured by a spectra colorimeter PR650 (purchased from Photo Research Inc.) and a luminance meter LS110 (purchased from Konica Minolta). The results are shown in Table 4.
Table 4
| measured at a brightness of 1000 Cd/m2 | driving voltage (V) | measured at a brightness of 1000 Cd/m2 | |||
| current efficiency (cd/A) | power efficiency (lm/W) | C.I.E coordinate | maximum luminous intensity peak (nm) | ||
| organic light-emitting device (X) | 44.8 | 39.2 | 3.6 | (0.51,0.46) | 580 |
| organic light-emitting device (XI) | 86.6 | 73.8 | 3.7 | (0.28,0.61) | 500 |
| organic light-emitting device (XII) | 64.0 | 53.8 | 3.7 | (0.42,0.56) | 544 |
| organic light-emitting device (XIII) | 86.6 | 68.3 | 4.1 | (0.41,0.58) | 540 |
| organic light-emitting device (XIV) | 62.5 | 51.6 | 3.8 | (0.32,0.62) | 520 |
| organic light-emitting device (XV) | 69.1 | 58.6 | 3.7 | (0.29,0.61) | 506 |
| organic light-emitting device (XVI) | 77.4 | 62.3 | 3.9 | (0.40,0.59) | 534 |
| organic light-emitting device (XVII) | 71.8 | 59.3 | 3.8 | (0.48,0.51) | 563 |
| organic light-emitting device (XIVIII) | 9.6 | 8.0 | 3.8 | (0.65,0.34) | 620 |
| organic light-emitting device (XIX) | 50.7 | 40.8 | 3.9 | (0.40,0.60) | 534 |
[0260] As shown in Table 4, during the formation of the light-emitting devices (X)-(XIII) via a dry process, it shows that the organic light-emitting device employing the organic metal compound having the structure of Formula (I) exhibits high luminous efficiency. Furthermore, the organic light-emitting device (XI) fabricated via the dry process has a current efficiency of 86.6 cd/A and a power efficiency of 73.8 lm/W.
1. An organic metal compound, having a structure of Formula I or Formula II:
wherein, R1 is independently hydrogen, C1-12 alkyl group, C1-12 alkoxy group, amine, C2-6 alkenyl group, C2-6 alkynyl group, C5-10 cycloalkyl group, C3-12 heteroaryl group, or C6-12 aryl group; R2, R3, R4, and R5 are independently hydrogen, halogen, C1-12 alkyl group, C1-12 alkoxy group, C1-12 fluoroalkyl group, or two adjacent groups of R2, R3, R4, and R5 are optionally combined with the carbon atoms which they are attached to, to form a cycloalkyl group, or aryl group; R6 and R7 are independent C1-6 alkyl group, or phenyl group; R8, R9, R10, and R11 are independently hydrogen, halogen, C1-12 alkyl group, C1-12 fluoroalkyl group, or two adjacent groups of R8, R9, R10, and R11 are optionally combined with the carbon atoms which they are attached to, to form a cycloalkyl group, or aryl group; R12, R13, R14, and R15 are independently hydrogen, halogen, C1-12 alkyl group, C1-12 fluoroalkyl group, or two adjacent groups of R12, R13, R14, and R15 are optionally combined with the carbon atoms which they are attached to, to form a cycloalkyl group, or aryl group; m is 1 or 2; and, n is 0 or 1.
wherein, R1 is independently hydrogen, C1-12 alkyl group, C1-12 alkoxy group, amine, C2-6 alkenyl group, C2-6 alkynyl group, C5-10 cycloalkyl group, C3-12 heteroaryl group, or C6-12 aryl group; R2, R3, R4, and R5 are independently hydrogen, halogen, C1-12 alkyl group, C1-12 alkoxy group, C1-12 fluoroalkyl group, or two adjacent groups of R2, R3, R4, and R5 are optionally combined with the carbon atoms which they are attached to, to form a cycloalkyl group, or aryl group; R6 and R7 are independent C1-6 alkyl group, or phenyl group; R8, R9, R10, and R11 are independently hydrogen, halogen, C1-12 alkyl group, C1-12 fluoroalkyl group, or two adjacent groups of R8, R9, R10, and R11 are optionally combined with the carbon atoms which they are attached to, to form a cycloalkyl group, or aryl group; R12, R13, R14, and R15 are independently hydrogen, halogen, C1-12 alkyl group, C1-12 fluoroalkyl group, or two adjacent groups of R12, R13, R14, and R15 are optionally combined with the carbon atoms which they are attached to, to form a cycloalkyl group, or aryl group; m is 1 or 2; and, n is 0 or 1.
2. The organic metal compound as claimed in claim 1, wherein the organic metal compound
is
R2, R3, R4, and R5 are independently hydrogen, halogen, C1-12 alkyl group, C1-12 alkoxy group, C1-12 fluoroalkyl group, or two adjacent groups of R2, R3, R4, and R5 are optionally combined with the carbon atoms which they are attached to, to form a cycloalkyl group, or aryl group; R6 and R7 are independent C1-6 alkyl group, or phenyl group; and, n is 0 or 1.
R2, R3, R4, and R5 are independently hydrogen, halogen, C1-12 alkyl group, C1-12 alkoxy group, C1-12 fluoroalkyl group, or two adjacent groups of R2, R3, R4, and R5 are optionally combined with the carbon atoms which they are attached to, to form a cycloalkyl group, or aryl group; R6 and R7 are independent C1-6 alkyl group, or phenyl group; and, n is 0 or 1.
3. The organic metal compound as claimed in claim 1, wherein the organic metal compound
is
or,
R1 is independently hydrogen, C1-12 alkyl group, C1-12 alkoxy group, amine, C2-6 alkenyl group, C2-6 alkynyl group, C5-10 cycloalkyl group, C3-12 heteroaryl group, or C6-12 aryl group; and, R2, R3, R4, and R5 are independently hydrogen, halogen, C1-12 alkyl group, C1-12 alkoxy group, C1-12 fluoroalkyl group, or two adjacent groups of R2, R3, R4, and R5 are optionally combined with the carbon atoms which they are attached to, to form a cycloalkyl group, or aryl group.
or,
R1 is independently hydrogen, C1-12 alkyl group, C1-12 alkoxy group, amine, C2-6 alkenyl group, C2-6 alkynyl group, C5-10 cycloalkyl group, C3-12 heteroaryl group, or C6-12 aryl group; and, R2, R3, R4, and R5 are independently hydrogen, halogen, C1-12 alkyl group, C1-12 alkoxy group, C1-12 fluoroalkyl group, or two adjacent groups of R2, R3, R4, and R5 are optionally combined with the carbon atoms which they are attached to, to form a cycloalkyl group, or aryl group.
4. The organic metal compound as claimed in claim 1, wherein
the organic metal compound is
R1 is independently hydrogen, C1-12 alkyl group, C1-12 alkoxy group, amine, C2-6 alkenyl group, C2-6 alkynyl group, C5-10 cycloalkyl group, C3-12 heteroaryl group, or C6-12 aryl group; and, R2, R3, R4, and R5 are independently hydrogen, halogen, C1-12 alkyl group, C1-12 alkoxy group, C1-12 fluoroalkyl group, or two adjacent groups of R2, R3, R4, and R5 are optionally combined with the carbon atoms which they are attached to, to form a cycloalkyl group, or aryl group, or wherein
the organic metal compound is
R1 is independently hydrogen, C1-12 alkyl group, C1-12 alkoxy group, amine, C2-6 alkenyl group, C2-6 alkynyl group, C5-10 cycloalkyl group, C3-12 heteroaryl group, or C6-12 aryl group; R2, R3, R4, and R5 are independently hydrogen, halogen, C1-12 alkyl group, C1-12 alkoxy group, C1-12 fluoroalkyl group, or two adjacent groups of R2, R3, R4, and R5 are optionally combined with the carbon atoms which they are attached to, to form a cycloalkyl group, or aryl group; and, m is 1 or 2.
the organic metal compound is
R1 is independently hydrogen, C1-12 alkyl group, C1-12 alkoxy group, amine, C2-6 alkenyl group, C2-6 alkynyl group, C5-10 cycloalkyl group, C3-12 heteroaryl group, or C6-12 aryl group; and, R2, R3, R4, and R5 are independently hydrogen, halogen, C1-12 alkyl group, C1-12 alkoxy group, C1-12 fluoroalkyl group, or two adjacent groups of R2, R3, R4, and R5 are optionally combined with the carbon atoms which they are attached to, to form a cycloalkyl group, or aryl group, or wherein
the organic metal compound is
R1 is independently hydrogen, C1-12 alkyl group, C1-12 alkoxy group, amine, C2-6 alkenyl group, C2-6 alkynyl group, C5-10 cycloalkyl group, C3-12 heteroaryl group, or C6-12 aryl group; R2, R3, R4, and R5 are independently hydrogen, halogen, C1-12 alkyl group, C1-12 alkoxy group, C1-12 fluoroalkyl group, or two adjacent groups of R2, R3, R4, and R5 are optionally combined with the carbon atoms which they are attached to, to form a cycloalkyl group, or aryl group; and, m is 1 or 2.
5. The organic metal compound as claimed in claim 1, wherein R8, R9, R10, and R11 are independently hydrogen, fluorine, methyl group, ethyl group, propyl group, isopropyl
group, n-butyl group, isobutyl group, tert-butyl group, pentyl group, hexyl group,
fluoromethyl, or fluoroethyl, or R9 and R10 are combined with the carbon atoms which they are attached to, to form a phenyl group,
and/or R10 and R11 are combined with the carbon atoms which they are attached to, to form a phenyl group.
6. The organic metal compound as claimed in claim 1, wherein the organic metal compound
is
R1 is independently hydrogen, C1-12 alkyl group, C1-12 alkoxy group, amine, C2-6 alkenyl group, C2-6 alkynyl group, C5-10 cycloalkyl group, C3-12 heteroaryl group, or C6-12 aryl group; R2, R3, R4, and R5 are independently hydrogen, halogen, C1-12 alkyl group, C1-12 alkoxy group, C1-12 fluoroalkyl group, or two adjacent groups of R2, R3, R4, and R5 are optionally combined with the carbon atoms which they are attached to, to form a cycloalkyl group, or aryl group; R12, R13, R14, and R15 are independently hydrogen, halogen, C1-12 alkyl group, C1-12 fluoroalkyl group, or two adjacent groups of R12, R13, R14, and R15 are optionally combined with the carbon atoms which they are attached to, to form a cycloalkyl group, or aryl group; and, m is 1 or 2.
R1 is independently hydrogen, C1-12 alkyl group, C1-12 alkoxy group, amine, C2-6 alkenyl group, C2-6 alkynyl group, C5-10 cycloalkyl group, C3-12 heteroaryl group, or C6-12 aryl group; R2, R3, R4, and R5 are independently hydrogen, halogen, C1-12 alkyl group, C1-12 alkoxy group, C1-12 fluoroalkyl group, or two adjacent groups of R2, R3, R4, and R5 are optionally combined with the carbon atoms which they are attached to, to form a cycloalkyl group, or aryl group; R12, R13, R14, and R15 are independently hydrogen, halogen, C1-12 alkyl group, C1-12 fluoroalkyl group, or two adjacent groups of R12, R13, R14, and R15 are optionally combined with the carbon atoms which they are attached to, to form a cycloalkyl group, or aryl group; and, m is 1 or 2.
7. The organic metal compound as claimed in claim 1, wherein the organic metal compound
is
R1 is independently hydrogen, C1-12 alkyl group, C1-12 alkoxy group, amine, C2-6 alkenyl group, C2-6 alkynyl group, C5-10 cycloalkyl group, C3-12 heteroaryl group, or C6-12 aryl group; R2, R3, R4, and R5 are independently hydrogen, halogen, C1-12 alkyl group, C1-12 alkoxy group, C1-12 fluoroalkyl group, or two adjacent groups of R2, R3, R4, and R5 are optionally combined with the carbon atoms which they are attached to, to form a cycloalkyl group, or aryl group; R12, R13, R14, and R15 are independently hydrogen, halogen, C1-12 alkyl group, C1-12 fluoroalkyl group, or two adjacent groups of R12, R13, R14, and R15 are optionally combined with the carbon atoms which they are attached to, to form a cycloalkyl group, or aryl group; and, m is 1 or 2.
R1 is independently hydrogen, C1-12 alkyl group, C1-12 alkoxy group, amine, C2-6 alkenyl group, C2-6 alkynyl group, C5-10 cycloalkyl group, C3-12 heteroaryl group, or C6-12 aryl group; R2, R3, R4, and R5 are independently hydrogen, halogen, C1-12 alkyl group, C1-12 alkoxy group, C1-12 fluoroalkyl group, or two adjacent groups of R2, R3, R4, and R5 are optionally combined with the carbon atoms which they are attached to, to form a cycloalkyl group, or aryl group; R12, R13, R14, and R15 are independently hydrogen, halogen, C1-12 alkyl group, C1-12 fluoroalkyl group, or two adjacent groups of R12, R13, R14, and R15 are optionally combined with the carbon atoms which they are attached to, to form a cycloalkyl group, or aryl group; and, m is 1 or 2.
8. The organic metal compound as claimed in claim 1, wherein R1 is independently hydrogen, or C1-12 alkyl group; R2, R3, R4, and R5 are independently hydrogen, halogen, C1-12 alkyl group, C1-12 alkoxy group, or two adjacent groups of R2, R3, R4, and R5 are optionally combined with the carbon atoms which they are attached to, to form
an aryl group; R6 and R7 are independent C1-6 alkyl group; R8, R9, R10, and R11 are independently hydrogen, C1-12 alkyl group, or two adjacent groups of R8, R9, R10, and R11 are optionally combined with the carbon atoms which they are attached to, to form
an aryl group; and R12, R13, R14, and R15 are independently hydrogen, or C1-12 alkyl group.
9. The organic metal compound as claimed in claim 1, wherein the organic metal compound
is
or
or
or
or
10. The organic metal compound as claimed in any of claims 1 or 3 to 7, wherein each R1 is independently hydrogen, methyl group, ethyl group, propyl group, isopropyl group,
n-butyl group, isobutyl group, tert-butyl group, pentyl group, hexyl group, cyclohexyl
group, phenyl group, biphenyl group, or naphthyl group.
11. The organic metal compound as claimed in any of claims 1 to 7, wherein
R2, R3, R4, and R5 are independently hydrogen, fluorine, methyl group, ethyl group, propyl group, isopropyl group, n-butyl group, isobutyl group, tert-butyl group, pentyl group, hexyl group, fluoromethyl, fluoroethyl, methoxy, ethoxy, propoxy, or isopropoxy, or R3 and R4 are combined with the carbon atoms which they are attached to, to form a phenyl group, or wherein
at least one of R1, R2, R3, R4, and R5 is not hydrogen.
R2, R3, R4, and R5 are independently hydrogen, fluorine, methyl group, ethyl group, propyl group, isopropyl group, n-butyl group, isobutyl group, tert-butyl group, pentyl group, hexyl group, fluoromethyl, fluoroethyl, methoxy, ethoxy, propoxy, or isopropoxy, or R3 and R4 are combined with the carbon atoms which they are attached to, to form a phenyl group, or wherein
at least one of R1, R2, R3, R4, and R5 is not hydrogen.
12. The organic metal compound as claimed in claims 1 or 2, wherein R6 and R7 are independently methyl group, ethyl group, propyl group, isopropyl group, n-butyl
group, isobutyl group, tert-butyl group, pentyl group, hexyl group, or phenyl group.
13. The organic metal compound as claimed in claims 1 or 5, wherein R8, R9, R10, and R11 are independently hydrogen, fluorine, methyl group, ethyl group, propyl group, isopropyl
group, n-butyl group, isobutyl group, tert-butyl group, pentyl group, hexyl group,
fluoromethyl, or fluoroethyl, or R9 and R10 are combined with the carbon atoms which they are attached to, to form a phenyl group,
and/or R10 and R11 are combined with the carbon atoms which they are attached to, to form a phenyl group.
14. The organic metal compound as claimed in claims 1, 6 or 7, wherein R12, R13, R14, and R15 are independently hydrogen, fluorine, methyl group, ethyl group, propyl group, isopropyl
group, n-butyl group, isobutyl group, tert-butyl group, pentyl group, hexyl group,
fluoromethyl, or fluoroethyl, or R12 and R13 are combined with the carbon atoms which they are attached to, to form a phenyl group,
and/or R13 and R14 are combined with the carbon atoms which they are attached to, to form a phenyl group.
15. An organic light-emitting device, comprising:
a pair of electrodes (14, 18); and
an organic light-emitting element (16), disposed between the electrodes (14, 18), wherein the organic light-emitting element (16) comprises the organic metal compound as claimed in claims 1 to 14.
1. Organische Metallverbindung mit einer Struktur der Formel I oder der Formel II:
wobei R1 unabhängig Wasserstoff, eine C1-12-Alkylgruppe, eine C1-12-Alkoxygruppe, Amin, eine C2-6-Alkenylgruppe, eine C2-6-Alkynylgruppe, eine C5-16-Cycloalkylgruppe, eine C3-12-Heteroarylgruppe oder eine C6-12-Arylgruppe ist, R2, R3, R4 und R5 unabhängig Wasserstoff, ein Halogen, eine C1-12-Alkylgruppe, eine C1-12-Alkoxygruppe, eine C1-12-Fluoralkylgruppe sind, oder wobei zwei benachbarte Gruppen von R2, R3, R4 und R5 optional über die Kohlenstoffatome kombiniert sind, mit denen sie verbunden sind, um eine Cycloalkylgruppe oder eine Arylgruppe zu bilden, R6 und R7 unabhängig eine C1-6-Alkylgruppe oder eine Phenylgruppe sind, R8, R9, R10 und R11 unabhängig Wasserstoff, ein Halogen, eine C1-12-Alkylgrupppe oder eine C1-12-Fluoralkylgruppe sind, oder wobei zwei benachbarte Gruppen von R8, R9, R10 und R11 optional über die Kohlenstoffatome kombiniert sind, mit denen sie verbunden sind, um eine Cycloalkylgruppe oder eine Arylgruppe zu bilden, R12, R13, R14 und R15 unabhängig Wasserstoff, ein Halogen, eine C1-12-Alkylgruppe oder eine C1-12-Fluoralkylgruppe sind, oder wobei zwei benachbarte Gruppen von R12, R13, R14 und R15 optional über die Kohlenstoffatome kombiniert sind, mit denen sie verbunden sind, um eine Cykloalkylgruppe oder eine Arylgruppe zu bilden, und wobei m = 1 oder 2 ist und n = 0 oder 1 ist.
wobei R1 unabhängig Wasserstoff, eine C1-12-Alkylgruppe, eine C1-12-Alkoxygruppe, Amin, eine C2-6-Alkenylgruppe, eine C2-6-Alkynylgruppe, eine C5-16-Cycloalkylgruppe, eine C3-12-Heteroarylgruppe oder eine C6-12-Arylgruppe ist, R2, R3, R4 und R5 unabhängig Wasserstoff, ein Halogen, eine C1-12-Alkylgruppe, eine C1-12-Alkoxygruppe, eine C1-12-Fluoralkylgruppe sind, oder wobei zwei benachbarte Gruppen von R2, R3, R4 und R5 optional über die Kohlenstoffatome kombiniert sind, mit denen sie verbunden sind, um eine Cycloalkylgruppe oder eine Arylgruppe zu bilden, R6 und R7 unabhängig eine C1-6-Alkylgruppe oder eine Phenylgruppe sind, R8, R9, R10 und R11 unabhängig Wasserstoff, ein Halogen, eine C1-12-Alkylgrupppe oder eine C1-12-Fluoralkylgruppe sind, oder wobei zwei benachbarte Gruppen von R8, R9, R10 und R11 optional über die Kohlenstoffatome kombiniert sind, mit denen sie verbunden sind, um eine Cycloalkylgruppe oder eine Arylgruppe zu bilden, R12, R13, R14 und R15 unabhängig Wasserstoff, ein Halogen, eine C1-12-Alkylgruppe oder eine C1-12-Fluoralkylgruppe sind, oder wobei zwei benachbarte Gruppen von R12, R13, R14 und R15 optional über die Kohlenstoffatome kombiniert sind, mit denen sie verbunden sind, um eine Cykloalkylgruppe oder eine Arylgruppe zu bilden, und wobei m = 1 oder 2 ist und n = 0 oder 1 ist.
2. Organische Metallverbindung nach Anspruch 1, wobei die organische Metallverbindung
ist, wobei R2, R3, R4 und R5 unabhängig Wasserstoff, ein Halogen, eine C1-12-Alkylgruppe, eine C1-12-Alkoxygruppe oder eine C1-12-Fluoralkylgruppe sind, oder wobei zwei benachbarte Gruppen von R2, R3, R4 und R5 optional über die Kohlenstoffatome kombiniert sind, mit denen sie verbunden sind, um eine Cycloalkylgruppe oder eine Arylgruppe zu bilden, R6 und R7 unabhängig eine C1-6-Alkylgruppe oder eine Phenylgruppe sind und n = 0 oder 1 ist.
ist, wobei R2, R3, R4 und R5 unabhängig Wasserstoff, ein Halogen, eine C1-12-Alkylgruppe, eine C1-12-Alkoxygruppe oder eine C1-12-Fluoralkylgruppe sind, oder wobei zwei benachbarte Gruppen von R2, R3, R4 und R5 optional über die Kohlenstoffatome kombiniert sind, mit denen sie verbunden sind, um eine Cycloalkylgruppe oder eine Arylgruppe zu bilden, R6 und R7 unabhängig eine C1-6-Alkylgruppe oder eine Phenylgruppe sind und n = 0 oder 1 ist.
3. Organische Metallverbindung nach Anspruch 1, wobei die organische Metallverbindung
oder
ist, wobei R1 unabhängig Wasserstoff, eine C1-12-Alkylgruppe, eine C1-12-Alkoxygruppe, Amin, eine C2-6-Alkenylgruppe, eine C2-6-Alkynylgruppe, eine C5-16-Cycloalkylgruppe, eine C3-12-Heteroarylgruppe oder eine C6-12-Arylgruppe ist, R2, R3, R4 und R5 unabhängig Wasserstoff, ein Halogen, eine C1-12-Alkylgruppe, eine C1-12-Alkoxygruppe oder eine C1-12-Fluoralkylgruppe sind, oder wobei zwei benachbarte Gruppen von R2, R3, R4 und R5 optional über die Kohlenstoffatome kombiniert sind, mit denen sie verbunden sind, um eine Cycloalkylgruppe oder eine Arylgruppe zu bilden.
oder
ist, wobei R1 unabhängig Wasserstoff, eine C1-12-Alkylgruppe, eine C1-12-Alkoxygruppe, Amin, eine C2-6-Alkenylgruppe, eine C2-6-Alkynylgruppe, eine C5-16-Cycloalkylgruppe, eine C3-12-Heteroarylgruppe oder eine C6-12-Arylgruppe ist, R2, R3, R4 und R5 unabhängig Wasserstoff, ein Halogen, eine C1-12-Alkylgruppe, eine C1-12-Alkoxygruppe oder eine C1-12-Fluoralkylgruppe sind, oder wobei zwei benachbarte Gruppen von R2, R3, R4 und R5 optional über die Kohlenstoffatome kombiniert sind, mit denen sie verbunden sind, um eine Cycloalkylgruppe oder eine Arylgruppe zu bilden.
4. Organische Metallverbindung nach Anspruch 1, wobei die organische Metallverbindung
ist, wobei R1 unabhängig Wasserstoff, eine C1-12-Alkylgruppe, eine C1-12-Alkoxygruppe, Amin, eine C2-6-Alkenylgruppe, eine C2-6-Alkynylgruppe, eine C5-10-Cycloalkylgruppe, eine C3-12-Heteroarylgruppe oder eine C6-12-Arylgruppe ist, R2, R3, R4 und R5 unabhängig Wasserstoff, ein Halogen, eine C1-12-Alkylgruppe, eine C1-12-Alkoxygruppe oder eine C1-12-Fluoralkylgruppe sind, oder wobei zwei benachbarte Gruppen von R2, R3, R4 und R5 optional über die Kohlenstoffatome kombiniert sind, mit denen sie verbunden sind, um eine Cycloalkylgruppe oder eine Arylgruppe zu bilden, und wobei m = 1 oder 2 ist.
ist, wobei R1 unabhängig Wasserstoff, eine C1-12-Alkylgruppe, eine C1-12-Alkoxygruppe, Amin, eine C2-6-Alkenylgruppe, eine C2-6-Alkynylgruppe, eine C5-10-Cycloalkylgruppe, eine C3-12-Heteroarylgruppe oder eine C6-12-Arylgruppe ist, R2, R3, R4 und R5 unabhängig Wasserstoff, ein Halogen, eine C1-12-Alkylgruppe, eine C1-12-Alkoxygruppe oder eine C1-12-Fluoralkylgruppe sind, oder wobei zwei benachbarte Gruppen von R2, R3, R4 und R5 optional über die Kohlenstoffatome kombiniert sind, mit denen sie verbunden sind, um eine Cycloalkylgruppe oder eine Arylgruppe zu bilden, und wobei m = 1 oder 2 ist.
5. Organische Metallverbindung nach Anspruch 1, wobei R8, R9, R10 und R11 unabhängig Wasserstoff, Fluor, eine Methylgruppe, eine Ethylgruppe, eine Propylgruppe,
eine Isopropylgruppe, eine n-Butylgruppe, eine Isobutylgruppe, eine tert-Butylgruppe,
eine Pentylgruppe, eine Hexylgruppe, Fluormethyl oder Fluorethyl sind, oder wobei
R9 und R10 über die Kohlenstoffatome kombiniert sind, mit denen sie verbunden sind, um eine
Phenylgruppe zu bilden, und/oder wobei R10 und R11 über die Kohlenstoffatome kombiniert sind, mit denen sie verbunden sind, um eine
Phenylgruppe zu bilden.
6. Organische Metallverbindung nach Anspruch 1, wobei die organische Metallverbindung
ist, wobei R1 unabhängig Wasserstoff, eine C1-12-Alkylgruppe, eine C1-12-Alkoxygruppe, Amin, eine C2-6-Alkenylgruppe, eine C2-6-Alkynylgruppe, eine C5-10-Cycloalkylgruppe, eine C3-12-Heteroarylgruppe oder eine C6-12-Arylgruppe ist, R2, R3, R4 und R5 unabhängig Wasserstoff, ein Halogen, eine C1-12-Alkylgruppe, eine C1-12-Alkoxygruppe oder eine C1-12-Fluoralkylgruppe sind, oder wobei zwei benachbarte Gruppen von R2, R3, R4 und R5 optional über die Kohlenstoffatome kombiniert sind, mit denen sie verbunden sind, um eine Cycloalkylgruppe oder eine Arylgruppe zu bilden, R12, R13, R14 und R15 unabhängig Wasserstoff, ein Halogen, eine C1-12-Alkylgruppe oder eine C1-12-Fluoralkylgruppe sind, oder wobei zwei benachbarte Gruppen von R12, R13, R14 und R15 optional über die Kohlenstoffatome kombiniert sind, mit denen sie verbunden sind, um eine Cykloalkylgruppe oder eine Arylgruppe zu bilden, und wobei m = 1 oder 2 ist.
ist, wobei R1 unabhängig Wasserstoff, eine C1-12-Alkylgruppe, eine C1-12-Alkoxygruppe, Amin, eine C2-6-Alkenylgruppe, eine C2-6-Alkynylgruppe, eine C5-10-Cycloalkylgruppe, eine C3-12-Heteroarylgruppe oder eine C6-12-Arylgruppe ist, R2, R3, R4 und R5 unabhängig Wasserstoff, ein Halogen, eine C1-12-Alkylgruppe, eine C1-12-Alkoxygruppe oder eine C1-12-Fluoralkylgruppe sind, oder wobei zwei benachbarte Gruppen von R2, R3, R4 und R5 optional über die Kohlenstoffatome kombiniert sind, mit denen sie verbunden sind, um eine Cycloalkylgruppe oder eine Arylgruppe zu bilden, R12, R13, R14 und R15 unabhängig Wasserstoff, ein Halogen, eine C1-12-Alkylgruppe oder eine C1-12-Fluoralkylgruppe sind, oder wobei zwei benachbarte Gruppen von R12, R13, R14 und R15 optional über die Kohlenstoffatome kombiniert sind, mit denen sie verbunden sind, um eine Cykloalkylgruppe oder eine Arylgruppe zu bilden, und wobei m = 1 oder 2 ist.
7. Organische Metallverbindung nach Anspruch 1, wobei die organische Metallverbindung
ist, wobei R1 unabhängig Wasserstoff, eine C1-12-Alkylgruppe, eine C1-12-Alkoxygruppe, Amin, eine C2-6-Alkenylgruppe, eine C2-6-Alkynylgruppe, eine C5-10-Cycloalkylgruppe, eine C3-12-Heteroarylgruppe oder eine C6-12-Arylgruppe ist, R2, R3, R4 und R5 unabhängig Wasserstoff, ein Halogen, eine C1-12-Alkylgruppe, eine C1-12-Alkoxygruppe oder eine C1-12-Fluoralkylgruppe sind, oder wobei zwei benachbarte Gruppen von R2, R3, R4 und R5 optional über die Kohlenstoffatome kombiniert sind, mit denen sie verbunden sind, um eine Cycloalkylgruppe oder eine Arylgruppe zu bilden, R12, R13, R14 und R15 unabhängig Wasserstoff, ein Halogen, eine C1-12-Alkylgruppe oder eine C1-12-Fluoralkylgruppe sind, oder wobei zwei benachbarte Gruppen von R12, R13, R14 und R15 optional über die Kohlenstoffatome kombiniert sind, mit denen sie verbunden sind, um eine Cykloalkylgruppe oder eine Arylgruppe zu bilden, und wobei m = 1 oder 2 ist.
ist, wobei R1 unabhängig Wasserstoff, eine C1-12-Alkylgruppe, eine C1-12-Alkoxygruppe, Amin, eine C2-6-Alkenylgruppe, eine C2-6-Alkynylgruppe, eine C5-10-Cycloalkylgruppe, eine C3-12-Heteroarylgruppe oder eine C6-12-Arylgruppe ist, R2, R3, R4 und R5 unabhängig Wasserstoff, ein Halogen, eine C1-12-Alkylgruppe, eine C1-12-Alkoxygruppe oder eine C1-12-Fluoralkylgruppe sind, oder wobei zwei benachbarte Gruppen von R2, R3, R4 und R5 optional über die Kohlenstoffatome kombiniert sind, mit denen sie verbunden sind, um eine Cycloalkylgruppe oder eine Arylgruppe zu bilden, R12, R13, R14 und R15 unabhängig Wasserstoff, ein Halogen, eine C1-12-Alkylgruppe oder eine C1-12-Fluoralkylgruppe sind, oder wobei zwei benachbarte Gruppen von R12, R13, R14 und R15 optional über die Kohlenstoffatome kombiniert sind, mit denen sie verbunden sind, um eine Cykloalkylgruppe oder eine Arylgruppe zu bilden, und wobei m = 1 oder 2 ist.
8. Organische Metallverbindung nach Anspruch 1, wobei R1 unabhängig Wasserstoff oder eine C1-12-Alkylgruppe ist, R2, R3, R4 und R5 unabhängig Wasserstoff, ein Halogen, eine C1-12-Alkylgruppe oder eine C1-12-Alkoxygruppe sind, oder wobei zwei benachbarte Gruppen von R2, R3, R4 und R5 optional über die Kohlenstoffatome kombiniert sind, mit denen sie verbunden sind,
um eine Arylgruppe zu bilden, R6 und R7 unabhängig eine C1-6-Alkylgruppe sind, R8, R9, R10 und R11 unabhängig Wasserstoff oder eine C1-12-Alkylgrupppe sind, oder wobei zwei benachbarte Gruppen von R8, R9, R10 und R11 optional über die Kohlenstoffatome kombiniert sind, mit denen sie verbunden sind,
um eine Arylgruppe zu bilden, und wobei R12, R13, R14 und R15 unabhängig Wasserstoff oder eine C1-12-Alkylgruppe sind.
9. Organische Metallverbindung nach Anspruch 1, wobei die organische Metallverbindung
oder
oder
ist.
oder
oder
ist.
10. Organische Metallverbindung nach einem der Ansprüche 1 oder 3 bis 7, wobei jede der
Komponenten R1 unabhängig Wasserstoff, eine Methylgruppe, eine Ethylgruppe, eine Propylgruppe, eine
Isopropylgruppe, eine n-Butylgruppe, eine Isobutylgruppe, eine tert-Butylgruppe, eine
Pentylgruppe, eine Hexylgruppe, eine Cyclohexylgruppe, eine Phenylgruppe, eine Biphenylgruppe
oder eine Naphthylgruppe ist.
11. Organische Metallverbindung nach einem der Ansprüche 1 bis 7, wobei
R2, R3, R4 und R5 unabhängig Wasserstoff, Fluor, eine Methylgruppe, eine Ethylgruppe, eine Propylgruppe, eine Isopropylgruppe, eine n-Butylgruppe, eine Isobutylgruppe, eine tert-Butylgruppe, eine Pentylgruppe, eine Hexylgruppe, Fluormethyl, Fluorethyl, Methoxy, Ethoxy, Propoxy oder Isopropoxy sind, oder wobei R3 und R4 über die Kohlenstoffatome kombiniert sind, mit denen sie verbunden sind, um eine Phenylgruppe zu bilden , oder wobei mindestens eine der Komponenten R1, R2, R3, R4 und R5 nicht Wasserstoff ist.
R2, R3, R4 und R5 unabhängig Wasserstoff, Fluor, eine Methylgruppe, eine Ethylgruppe, eine Propylgruppe, eine Isopropylgruppe, eine n-Butylgruppe, eine Isobutylgruppe, eine tert-Butylgruppe, eine Pentylgruppe, eine Hexylgruppe, Fluormethyl, Fluorethyl, Methoxy, Ethoxy, Propoxy oder Isopropoxy sind, oder wobei R3 und R4 über die Kohlenstoffatome kombiniert sind, mit denen sie verbunden sind, um eine Phenylgruppe zu bilden , oder wobei mindestens eine der Komponenten R1, R2, R3, R4 und R5 nicht Wasserstoff ist.
12. Organische Metallverbindung Anspruch 1 oder 2, wobei R6 und R7 unabhängig eine Methylgruppe, eine Ethylgruppe, eine Propylgruppe, eine Isopropylgruppe,
eine n-Butylgruppe, eine Isobutylgruppe, eine tert-Butylgruppe, eine Pentylgruppe,
eine Hexylgruppe oder eine Phenylgruppe sind.
13. Organische Metallverbindung nach Anspruch 1 oder 5, wobei R8, R9, R10 und R11 unabhängig Wasserstoff, Fluor, eine Methylgruppe, eine Ethylgruppe, eine Propylgruppe,
eine Isopropylgruppe, eine n-Butylgruppe, eine Isobutylgruppe, eine tert-Butylgruppe,
eine Pentylgruppe, eine Hexylgruppe, Fluormethyl oder Fluorethyl sind, oder wobei
R9 und R10 über die Kohlenstoffatome kombiniert sind, mit denen sie verbunden sind, um eine
Phenylgruppe zu bilden, und/oder wobei R10 und R11 über die Kohlenstoffatome kombiniert sind, mit denen sie verbunden sind, um eine
Phenylgruppe zu bilden.
14. Organische Metallverbindung nach Anspruch 1, 6 oder 7, wobei R12, R13, R14 und R15 unabhängig Wasserstoff, Fluor, eine Methylgruppe, eine Ethylgruppe, eine Propylgruppe,
eine Isopropylgruppe, eine n-Butylgruppe, eine Isobutylgruppe, eine tert-Butylgruppe,
eine Pentylgruppe, eine Hexylgruppe, Fluormethyl oder Fluorethyl sind, oder wobei
R12 und R13 über die Kohlenstoffatome kombiniert sind, mit denen sie verbunden sind, um eine
Phenylgruppe zu bilden, und/oder wobei R13 und R14 über die Kohlenstoffatome kombiniert sind, mit denen sie verbunden sind, um eine
Phenylgruppe zu bilden.
15. Organisches lichtemittierendes Bauelement, mit:
einem Paar Elektroden (14, 18); und
einem zwischen den Elektroden (14, 18) angeordneten organischen lichtemittierenden Element (16), wobei das organische lichtemittierende Element (16) die organische Metallverbindung nach einem der Ansprüche 1 bis 14 aufweist.
1. Composé organométallique, ayant une structure selon la Formule I ou la Formule II
:
où R1 est indépendamment un atome d'hydrogène, un groupe alkyle en C1-12, un groupe alcoxy en C1-12, un groupe amine, un groupe alcényle en C2-6, un groupe alcynyle en C2-6, un groupe cycloalkyle en C5-10, un groupe hétéroaryle en C3-12, ou un groupe aryle en C6-12 ; R2, R3, R4 et R5 sont indépendamment un atome d'hydrogène, d'halogène, un groupe alkyle en C1-12, un groupe alcoxy en C1-12, un groupe fluoro alkyle en C1-12, ou deux groupes adjacents de R2, R3, R4 et R5 sont éventuellement combinés avec les atomes de carbone auxquels ils sont rattachés pour former un groupe cycloalkyle, ou un groupe aryle ; R6 et R7 sont indépendamment un groupe alkyle en C1-6, ou un groupe phényle ; R8, R9, R10 et R11 sont indépendamment un atome d'hydrogène, d'halogène, un groupe alkyle en C1-12, un groupe fluoro alkyle en C1-12, ou deux groupes adjacents de R8, R9, R10 et R11 sont éventuellement combinés avec les atomes de carbone auxquels ils sont rattachés pour former un groupe cycloalkyle, ou un groupe aryle ; R12, R13, R14 et R15 sont indépendamment un atome d'hydrogène, d'halogène, un groupe alkyle en C1-12, un groupe fluoro alkyle en C1-12, ou deux groupes adjacents de R12, R13, R14 et R15 sont éventuellement combinés avec les atomes de carbone auxquels ils sont rattachés pour former un groupe cycloalkyle, ou un groupe aryle ; m est égal à 1 ou 2 ; et n est égal à 0 ou 1.
où R1 est indépendamment un atome d'hydrogène, un groupe alkyle en C1-12, un groupe alcoxy en C1-12, un groupe amine, un groupe alcényle en C2-6, un groupe alcynyle en C2-6, un groupe cycloalkyle en C5-10, un groupe hétéroaryle en C3-12, ou un groupe aryle en C6-12 ; R2, R3, R4 et R5 sont indépendamment un atome d'hydrogène, d'halogène, un groupe alkyle en C1-12, un groupe alcoxy en C1-12, un groupe fluoro alkyle en C1-12, ou deux groupes adjacents de R2, R3, R4 et R5 sont éventuellement combinés avec les atomes de carbone auxquels ils sont rattachés pour former un groupe cycloalkyle, ou un groupe aryle ; R6 et R7 sont indépendamment un groupe alkyle en C1-6, ou un groupe phényle ; R8, R9, R10 et R11 sont indépendamment un atome d'hydrogène, d'halogène, un groupe alkyle en C1-12, un groupe fluoro alkyle en C1-12, ou deux groupes adjacents de R8, R9, R10 et R11 sont éventuellement combinés avec les atomes de carbone auxquels ils sont rattachés pour former un groupe cycloalkyle, ou un groupe aryle ; R12, R13, R14 et R15 sont indépendamment un atome d'hydrogène, d'halogène, un groupe alkyle en C1-12, un groupe fluoro alkyle en C1-12, ou deux groupes adjacents de R12, R13, R14 et R15 sont éventuellement combinés avec les atomes de carbone auxquels ils sont rattachés pour former un groupe cycloalkyle, ou un groupe aryle ; m est égal à 1 ou 2 ; et n est égal à 0 ou 1.
2. Composé organométallique selon la revendication 1, dans lequel le composé organométallique
est
R2, R3, R4 et R5 sont indépendamment un atome d'hydrogène, d'halogène, un groupe alkyle en C1-12, un groupe alcoxy en C1-12, un groupe fluoro alkyle en C1-12, ou deux groupes adjacents de R2, R3, R4 et R5 sont éventuellement combinés avec les atomes de carbone auxquels ils sont rattachés pour former un groupe cycloalkyle, ou un groupe aryle ; R6 et R7 sont indépendamment un groupe alkyle en C1-6, ou un groupe phényle ; et n est égal à 0 ou 1.
R2, R3, R4 et R5 sont indépendamment un atome d'hydrogène, d'halogène, un groupe alkyle en C1-12, un groupe alcoxy en C1-12, un groupe fluoro alkyle en C1-12, ou deux groupes adjacents de R2, R3, R4 et R5 sont éventuellement combinés avec les atomes de carbone auxquels ils sont rattachés pour former un groupe cycloalkyle, ou un groupe aryle ; R6 et R7 sont indépendamment un groupe alkyle en C1-6, ou un groupe phényle ; et n est égal à 0 ou 1.
3. Composé organométallique selon la revendication 1, dans lequel le composé organométallique
est
ou
R1 est indépendamment un atome d'hydrogène, un groupe alkyle en C1-12, un groupe alcoxy en C1-12, un groupe amine, un groupe alcényle en C2-6, un groupe alcynyle en C2-6, un groupe cycloalkyle en C5-10, un groupe hétéroaryle en C3-12, ou un groupe aryle en C6-12 ; et R2, R3, R4 et R5 sont indépendamment un atome d'hydrogène, d'halogène, un groupe alkyle en C1-12, un groupe alcoxy en C1-12, un groupe fluoro alkyle en C1-12, ou deux groupes adjacents de R2, R3, R4 et R5 sont éventuellement combinés avec les atomes de carbone auxquels ils sont rattachés pour former un groupe cycloalkyle, ou un groupe aryle.
ou
R1 est indépendamment un atome d'hydrogène, un groupe alkyle en C1-12, un groupe alcoxy en C1-12, un groupe amine, un groupe alcényle en C2-6, un groupe alcynyle en C2-6, un groupe cycloalkyle en C5-10, un groupe hétéroaryle en C3-12, ou un groupe aryle en C6-12 ; et R2, R3, R4 et R5 sont indépendamment un atome d'hydrogène, d'halogène, un groupe alkyle en C1-12, un groupe alcoxy en C1-12, un groupe fluoro alkyle en C1-12, ou deux groupes adjacents de R2, R3, R4 et R5 sont éventuellement combinés avec les atomes de carbone auxquels ils sont rattachés pour former un groupe cycloalkyle, ou un groupe aryle.
4. Composé organométallique selon la revendication 1, dans lequel le composé organométallique
est
R1 est indépendamment un atome d'hydrogène, un groupe alkyle en C1-12, un groupe alcoxy en C1-12, un groupe amine, un groupe alcényle en C2-6, un groupe alcynyle en C2-6, un groupe cycloalkyle en C5-10, un groupe hétéroaryle en C3-12, ou un groupe aryle en C6-12 ; et R2, R3, R4 et R5 sont indépendamment un atome d'hydrogène, d'halogène, un groupe alkyle en C1-12, un groupe alcoxy en C1-12, un groupe fluoro alkyle en C1-12, ou deux groupes adjacents de R2, R3, R4 et R5 sont éventuellement combinés avec les atomes de carbone auxquels ils sont rattachés pour former un groupe cycloalkyle, ou un groupe aryle, ou dans lequel le composé organométallique est
R1 est indépendamment un atome d'hydrogène, un groupe alkyle en C1-12, un groupe alcoxy en C1-12, un groupe amine, un groupe alcényle en C2-6, un groupe alcynyle en C2-6, un groupe cycloalkyle en C5-10, un groupe hétéroaryle en C3-12, ou un groupe aryle en C6-12 ; R2, R3, R4 et R5 sont indépendamment un atome d'hydrogène, d'halogène, un groupe alkyle en C1-12, un groupe alcoxy en C1-12, un groupe fluoro alkyle en C1-12, ou deux groupes adjacents de R2, R3, R4 et R5 sont éventuellement combinés avec les atomes de carbone auxquels ils sont rattachés pour former un groupe cycloalkyle, ou un groupe aryle ; et m est égal à 1 ou 2.
R1 est indépendamment un atome d'hydrogène, un groupe alkyle en C1-12, un groupe alcoxy en C1-12, un groupe amine, un groupe alcényle en C2-6, un groupe alcynyle en C2-6, un groupe cycloalkyle en C5-10, un groupe hétéroaryle en C3-12, ou un groupe aryle en C6-12 ; et R2, R3, R4 et R5 sont indépendamment un atome d'hydrogène, d'halogène, un groupe alkyle en C1-12, un groupe alcoxy en C1-12, un groupe fluoro alkyle en C1-12, ou deux groupes adjacents de R2, R3, R4 et R5 sont éventuellement combinés avec les atomes de carbone auxquels ils sont rattachés pour former un groupe cycloalkyle, ou un groupe aryle, ou dans lequel le composé organométallique est
R1 est indépendamment un atome d'hydrogène, un groupe alkyle en C1-12, un groupe alcoxy en C1-12, un groupe amine, un groupe alcényle en C2-6, un groupe alcynyle en C2-6, un groupe cycloalkyle en C5-10, un groupe hétéroaryle en C3-12, ou un groupe aryle en C6-12 ; R2, R3, R4 et R5 sont indépendamment un atome d'hydrogène, d'halogène, un groupe alkyle en C1-12, un groupe alcoxy en C1-12, un groupe fluoro alkyle en C1-12, ou deux groupes adjacents de R2, R3, R4 et R5 sont éventuellement combinés avec les atomes de carbone auxquels ils sont rattachés pour former un groupe cycloalkyle, ou un groupe aryle ; et m est égal à 1 ou 2.
5. Composé organométallique selon la revendication 1, dans lequel R8, R9, R10 et R11 sont indépendamment un atome d'hydrogène, de fluor, un groupe méthyle, un groupe
éthyle, un groupe propyle, un groupe isopropyle, un groupe n-butyle, un groupe isobutyle,
un groupe tert-butyle, un groupe pentyle, un groupe hexyle, un groupe fluoro méthyle,
ou fluoro éthyle, ou R9 et R10 sont combinés avec les atomes de carbone auxquels ils sont rattachés pour former
un groupe phényle, et/ou R10 et R11 sont combinés avec les atomes de carbone auxquels ils sont rattachés pour former
un groupe phényle.
6. Composé organométallique selon la revendication 1, où le composé organométallique
est
R1 est indépendamment un atome d'hydrogène, un groupe alkyle en C1-12, un groupe alcoxy en C1-12, un groupe amine, un groupe alcényle en C2-6, un groupe alcynyle en C2-6, un groupe cycloalkyle en C5-10, un groupe hétéroaryle en C3-12, ou un groupe aryle en C6-12 ; R2, R3, R4 et R5 sont indépendamment un atome d'hydrogène, d'halogène, un groupe alkyle en C1-12, un groupe alcoxy en C1-12, un groupe fluoro alkyle en C1-12, ou deux groupes adjacents de R2, R3, R4 et R5 sont éventuellement combinés avec les atomes de carbone auxquels ils sont rattachés pour former un groupe cycloalkyle, ou un groupe aryle ; R12, R13, R14 et R15 sont indépendamment un atome d'hydrogène, d'halogène, un groupe alkyle en C1-12, un groupe fluoro alkyle en C1-12, ou deux groupes adjacents de R12, R13, R14 et R15 sont éventuellement combinés avec les atomes de carbone auxquels ils sont rattachés pour former un groupe cycloalkyle, ou un groupe aryle ; et m est égal à 1 ou 2.
R1 est indépendamment un atome d'hydrogène, un groupe alkyle en C1-12, un groupe alcoxy en C1-12, un groupe amine, un groupe alcényle en C2-6, un groupe alcynyle en C2-6, un groupe cycloalkyle en C5-10, un groupe hétéroaryle en C3-12, ou un groupe aryle en C6-12 ; R2, R3, R4 et R5 sont indépendamment un atome d'hydrogène, d'halogène, un groupe alkyle en C1-12, un groupe alcoxy en C1-12, un groupe fluoro alkyle en C1-12, ou deux groupes adjacents de R2, R3, R4 et R5 sont éventuellement combinés avec les atomes de carbone auxquels ils sont rattachés pour former un groupe cycloalkyle, ou un groupe aryle ; R12, R13, R14 et R15 sont indépendamment un atome d'hydrogène, d'halogène, un groupe alkyle en C1-12, un groupe fluoro alkyle en C1-12, ou deux groupes adjacents de R12, R13, R14 et R15 sont éventuellement combinés avec les atomes de carbone auxquels ils sont rattachés pour former un groupe cycloalkyle, ou un groupe aryle ; et m est égal à 1 ou 2.
7. Composé organométallique selon la revendication 1, où le composé organométallique
est
R1 est indépendamment un atome d'hydrogène, un groupe alkyle en C1-12, un groupe alcoxy en C1-12, un groupe amine, un groupe alcényle en C2-6, un groupe alcynyle en C2-6, un groupe cycloalkyle en C5-10, un groupe hétéroaryle en C3-12, ou un groupe aryle en C6-12 ; R2, R3, R4 et R5 sont indépendamment un atome d'hydrogène, d'halogène, un groupe alkyle en C1-12, un groupe alcoxy en C1-12, un groupe fluoro alkyle en C1-12, ou deux groupes adjacents de R2 , R3, R4 et R5 sont éventuellement combinés avec les atomes de carbone auxquels ils sont rattachés pour former un groupe cycloalkyle, ou un groupe aryle ; R12, R13, R14 et R15 sont indépendamment un atome d'hydrogène, d'halogène, un groupe alkyle en C1-12, un groupe fluoro alkyle en C1-12, ou deux groupes adjacents de R12, R13, R14 et R15 sont éventuellement combinés avec les atomes de carbone auxquels ils sont rattachés pour former un groupe cycloalkyle, ou un groupe aryle ; et m est égal à 1 ou 2.
R1 est indépendamment un atome d'hydrogène, un groupe alkyle en C1-12, un groupe alcoxy en C1-12, un groupe amine, un groupe alcényle en C2-6, un groupe alcynyle en C2-6, un groupe cycloalkyle en C5-10, un groupe hétéroaryle en C3-12, ou un groupe aryle en C6-12 ; R2, R3, R4 et R5 sont indépendamment un atome d'hydrogène, d'halogène, un groupe alkyle en C1-12, un groupe alcoxy en C1-12, un groupe fluoro alkyle en C1-12, ou deux groupes adjacents de R2 , R3, R4 et R5 sont éventuellement combinés avec les atomes de carbone auxquels ils sont rattachés pour former un groupe cycloalkyle, ou un groupe aryle ; R12, R13, R14 et R15 sont indépendamment un atome d'hydrogène, d'halogène, un groupe alkyle en C1-12, un groupe fluoro alkyle en C1-12, ou deux groupes adjacents de R12, R13, R14 et R15 sont éventuellement combinés avec les atomes de carbone auxquels ils sont rattachés pour former un groupe cycloalkyle, ou un groupe aryle ; et m est égal à 1 ou 2.
8. Composé organométallique selon la revendication 1, dans lequel R1 est indépendamment un atome d'hydrogène ou un groupe alkyle en C1-12 ; R2, R3, R4 et R5 sont indépendamment un atome d'hydrogène, d'halogène, un groupe alkyle en C1-12, un groupe alcoxy en C1-12, ou deux groupes adjacents de R2, R3, R4 et R5 sont éventuellement combinés avec les atomes de carbone auxquels ils sont rattachés
pour former un groupe aryle ; R6 et R7 sont indépendamment un groupe alkyle en C1-6 ; R8, R9, R10 et R11 sont indépendamment un atome d'hydrogène, un groupe alkyle en C1-12, ou deux groupes adjacents de R8, R9, R10 et R11 sont éventuellement combinés avec les atomes de carbone auxquels ils sont rattachés
pour former un groupe aryle ; et R12, R13, R14 et R15 sont indépendamment un atome d'hydrogène ou un groupe alkyle en C1-12.
9. Composé organométallique selon la revendication 1, où le composé organométallique
est
ou
ou
ou
ou
10. Composé organométallique selon l'une quelconque des revendications 1 ou 3 à 7, dans
lequel chaque R1 est indépendamment un atome d'hydrogène, un groupe méthyle, un groupe éthyle, un
groupe propyle, un groupe isopropyle, un groupe n-butyle, un groupe isobutyle, un
groupe tert-butyle, un groupe pentyle, un groupe hexyle, un groupe cyclohexyle, un
groupe phényle, un groupe biphényle ou un groupe naphtyle.
11. Composé organométallique selon l'une quelconque des revendications 1 à 7, dans lequel
R2, R3, R4 et R5 sont indépendamment un atome d'hydrogène, de fluor, un groupe méthyle, un groupe
éthyle, un groupe propyle, un groupe isopropyle, un groupe n-butyle, un groupe isobutyle,
un groupe tert-butyle, un groupe pentyle, un groupe hexyle, un groupe fluoro méthyle,
un groupe fluoro éthyle, un groupe méthoxy, éthoxy, propoxy ou isopropoxy, ou R3 et R4 sont combinés avec les atomes de carbone auxquels ils sont rattachés pour former
un groupe phényle ou dans lequel
au moins l'un parmi R1, R2, R3, R4 et R5 n'est pas un atome d'hydrogène.
au moins l'un parmi R1, R2, R3, R4 et R5 n'est pas un atome d'hydrogène.
12. Composé organométallique selon la revendication 1 ou 2, dans lequel R6 et R7 sont indépendamment un groupe méthyle, un groupe éthyle, un groupe propyle, un groupe
isopropyle, un groupe n-butyle, un groupe isobutyle, un groupe tert-butyle, un groupe
pentyle, un groupe hexyle ou un groupe phényle.
13. Composé organométallique selon les revendications 1 ou 5, dans lequel R8, R9, R10 et R11 sont indépendamment un atome d'hydrogène, de fluor, un groupe méthyle, un groupe
éthyle, un groupe propyle, un groupe isopropyle, un groupe n-butyle, un groupe isobutyle,
un groupe tert-butyle, un groupe pentyle, un groupe hexyle, un groupe fluoro méthyle
ou fluoro éthyle, ou R9 et R10 sont combinés avec les atomes de carbone auxquels ils sont rattachés pour former
un groupe phényle, et/ou R10 et R11 sont combinés avec les atomes de carbone auxquels ils sont rattachés pour former
un groupe phényle.
14. Composé organométallique selon les revendications 1, 6 ou 7, dans lequel R12, R13, R14 et R15 sont indépendamment un atome d'hydrogène, de fluor, un groupe méthyle, un groupe
éthyle, un groupe propyle, un groupe isopropyle, un groupe n-butyle, un groupe isobutyle,
un groupe tert-butyle, un groupe pentyle, un groupe hexyle, un groupe fluoro méthyle
ou fluoro éthyle, ou R12 et R13 sont combinés avec les atomes de carbone auxquels ils sont rattachés pour former
un groupe phényle, et/ou R13 et R14 sont combinés avec les atomes de carbone auxquels ils sont rattachés pour former
un groupe phényle.
15. Dispositif électroluminescent organique comprenant :
une paire d'électrodes (14, 18) ; et
un élément électroluminescent organique (16), disposé entre les électrodes (14, 18),
où l'élément électroluminescent organique (16) comprend le composé organométallique selon les revendications 1 à 14.
REFERENCES CITED IN THE DESCRIPTION
This list of references cited by the applicant is for the reader's convenience only. It does not form part of the European patent document. Even though great care has been taken in compiling the references, errors or omissions cannot be excluded and the EPO disclaims all liability in this regard.
Patent documents cited in the description